(Q33699908)

28 July 2017

1 reference

title

Loss of heterozygosity in human skin (English)

1 reference

28 July 2017

1 reference

Happle R

1

1 reference

28 July 2017

language of work or name

English

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publication date

1 August 1999

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Journal of the American Academy of Dermatology

28 July 2017

published in

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28 July 2017

volume

41

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28 July 2017

issue

2 Pt 1

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28 July 2017

page(s)

143-164

1 reference

Mechanisms of loss of heterozygosity in retinoblastoma

28 July 2017

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7 January 2021

Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders

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7 January 2021

Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis

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7 January 2021

CYTOLOGICAL EVIDENCE FOR CROSSING-OVER IN VITRO IN HUMAN LYMPHOID CELLS.

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7 January 2021

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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7 January 2021

Molecular evidence that homologous recombination occurs in proliferating human somatic cells

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7 January 2021

Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma

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7 January 2021

Telomeres, hidden mosaicism, loss of heterozygosity, and complex genetic traits

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7 January 2021

A general theory of carcinogenesis

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7 January 2021

A two-stage theory of carcinogenesis in relation to the age distribution of human cancer

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7 January 2021

Mutation and cancer: statistical study of retinoblastoma

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7 January 2021

Mutation and childhood cancer: a probabilistic model for the incidence of retinoblastoma

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7 January 2021

Model for the incidence of embryonal cancers: application to retinoblastoma

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7 January 2021

Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome

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7 January 2021

Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus

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7 January 2021

Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9

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https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Chromosome 9 allele loss occurs in both basal and squamous cell carcinomas of the skin

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https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer

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https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Genetic instability in the 9q22.3 region is a late event in the development of squamous cell carcinoma

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https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity in sporadic primary cutaneous melanoma

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https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Mutational analysis of the human p53 gene in malignant melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Homozygous deletions within human chromosome band 9p21 in melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

p16INK4a expression is frequently decreased and associated with 9p21 loss of heterozygosity in sporadic melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Prognostic significance of allelic losses in primary melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Retention of theCDKN2A locus and low frequency of point mutations in primary and metastasic cutaneous malignant melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Identification of PTEN/MMAC1 alterations in uncultured melanomas and melanoma cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

In vitro loss of heterozygosity targets the PTEN/MMAC1 gene in melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Microsatellite instability in malignant melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Comparison of genetic profiles between primary melanomas and their metastases reveals genetic alterations and clonal evolution during progression

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Genetic changes associated with primary Merkel cell carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Frequent allelic losses on chromosome 13q in human male breast carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Frequent loss of heterozygosity at chromosome 13q12-13 with BRCA2 markers in sporadic male breast cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Nevoid basal cell carcinoma syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

A two-hit model for developmental defects in Gorlin syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Human homolog of patched, a candidate gene for the basal cell nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Mutations affecting segment number and polarity in Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

A protein with several possible membrane-spanning domains encoded by the Drosophila segment polarity gene patched

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

The Drosophila patched gene encodes a putative membrane protein required for segmental patterning

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Is human patched the gatekeeper of common skin cancers?

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Tumour suppressors. Dispatches from patched

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Mutations in the human homologue of the Drosophila patched gene in esophageal squamous cell carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Patching together the genetics of Gorlin syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Origin of familial malignant melanomas from heritable melanocytic lesions. 'The B-K mole syndrome'

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https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Acquired precursors of cutaneous malignant melanoma. The familial dysplastic nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Arguments in favor of a polygenic inheritance of precursor nevi

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity detected on 1p and 9q in microdissected atypical nevi

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Concordance of genetic changes in basal cell carcinoma and associated clusters of squamous cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity analysis of keratoacanthoma reveals multiple differences from cutaneous squamous cell carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity at 5q21-22 (adenomatous polyposis coli gene region) in oral squamous cell carcinoma is common and correlated with advanced disease

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

p53 alterations in betel quid- and tobacco-associated oral squamous cell carcinomas from Taiwan.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Pediatric brain tumors: loss of heterozygosity at 17p and TP53 gene mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity of 3p markers in neuroblastoma tumours implicate a tumour-suppressor locus distal to the FHIT gene

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Molecular definition of chromosome translocations involving 10q24 and 19q13 in human malignant glioma cells

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Heterogeneity of mesothelioma cell lines as defined by altered genomic structure and expression of the NF2 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

1 reference

7 January 2021

Loss of heterozygosity on chromosome 11p15 during histological progression in microdissected ductal carcinoma of the breast

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Frequent loss of heterozygosity and three critical regions on the short arm of chromosome 8 in ovarian adenocarcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity on chromosome 6q27 and p53 mutations in epithelial ovarian cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Novel point mutations and allele loss at the RET locus in sporadic medullary thyroid carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Genetic analysis of lung tumours of non-smoking subjects: p53 gene mutations are constantly associated with loss of heterozygosity at the FHIT locus

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity in the tuberous sclerosis gene associated regions in adenocarcinoma of the lung accompanied by multiple atypical adenomatous hyperplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Sequential loss of heterozygosity in the progression of squamous cell carcinoma of the lung

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity and microsatellite instability in de novo versus ex-adenoma carcinomas of the colorectum

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Genetic alterations in colorectal cancer, comparative analysis of deletion events, and point mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity in the region including the BRCA1 gene on 17q in colon cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity and loss of expression of the DCC gene in gastric cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Cytogenetic and FISH analyses of pancreatic carcinoma reveal breaks in 18q11 with consistent loss of 18q12-qter and frequent gain of 18p.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Allelic loss on chromosome 9 in bladder cancer tissues and urine samples detected by blunt-end single-strand DNA conformation polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of p16/INK4A protein expression in non-Hodgkin's lymphomas is a frequent finding associated with tumor progression

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

A search for novel tumour suppressor genes for adult acute leukaemia by allelotyping at sub-telomeric chromosomal regions

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

NF1: a prevalent cause of tumorigenesis in human cancers?

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity of NF1 gene in juvenile chronic myelogenous leukemia with neurofibromatosis type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Genomic imprinting and gene activation in cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

p53 gene mutation and loss of heterozygosity of chromosome 11 in methylcholanthrene-induced mouse sarcomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Non-random allelic losses at 3p, 11p and 13q during HPV-mediated immortalization and concomitant loss of terminal differentiation of human keratinocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity in tuberous sclerosis hamartomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Cutaneous tumors in patients with multiple endocrine neoplasia type 1 show allelic deletion of the MEN1 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large family

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Somatic NF2 gene mutations in familial and non-familial vestibular schwannoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Clonal analysis by chromosome 11 microsatellite-PCR of microdissected parathyroid tumors from MEN 1 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of the NF2 gene and merlin occur by the tumorlet stage of schwannoma development in neurofibromatosis 2

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

MEN1 gene mutations in 12 MEN1 families and their associated tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Alleles of APC modulate the frequency and classes of mutations that lead to colon polyps

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Multiple endocrine neoplasia type 1: clinical and genetic topics

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

The tuberous sclerosis gene on chromosome 9q34 acts as a growth suppressor

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Evidence that lymphangiomyomatosis is caused by TSC2 mutations: chromosome 16p13 loss of heterozygosity in angiomyolipomas and lymph nodes from women with lymphangiomyomatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Ultraviolet-induced acute histological changes in irradiated nevi are not associated with allelic loss

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Segmental forms of autosomal dominant skin disorders: different types of severity reflect different states of zygosity

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

A rule concerning the segmental manifestation of autosomal dominant skin disorders. Review of clinical examples providing evidence for dichotomous types of severity

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Congenital ichthyosiform erythroderma and epidermal nevus

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Relapsing linear acantholytic dermatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Linear Porokeratosis in a Family With DSAP

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Cytogenetic studies in a patient with porokeratosis of Mibelli, multiple cancers and a forme fruste of Werner's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Disseminated superficial actinic porokeratosis. Coexistence with other porokeratotic variants

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Linear porokeratosis in two families with disseminated superficial actinic porokeratosis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Scaly atrophic lesions both scattered and in linear arrays. Disseminated superficial actinic porokeratosis in a patient with linear porokeratosis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Porokeratosis and Crohn's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Somatic recombination may explain linear porokeratosis associated with disseminated superficial actinic porokeratosis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Cancer proneness of linear porokeratosis may be explained by allelic loss

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

MULTIPLE CUTANEOUS LEIOMYOMA IN IDENTICAL TWINS

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Segmentary and disseminated lesions in multiple hereditary cutaneous leiomyoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

An Unusual Case of Preponderantly Right-Sided Syringomas

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Plaque type syringoma

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

1 reference

7 January 2021

Diffuse and progressive nodular plaques

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Dyskeratosis congenita with linear areas of severe cutaneous involvement

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

1 reference

7 January 2021

Somatic recombination may explain linear psoriasis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Evidence for loss of heterozygosity in human psoriatic lesions

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Linear pustular psoriasis that developed in a patient with generalized pustular psoriasis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Linear atopic dermatitis ('naevus atopicus'): a pathogenetic clue?

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Zosteriform lichen planus

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Linear lichenoid graft-vs-host disease

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Dermatomal lichenoid chronic graft-vs-host disease following varicella-zoster infection despite absence of viral genome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Localized linear bullous eruption of systemic lupus erythematosus in a child

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Linear pemphigus vulgaris after X-ray irradiation

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Mosaic atopic eczema cured by autotransplantation?

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Multiple linear lichen planus in the lines of Blaschko

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Linear chronic cutaneous graft-versus-host disease

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Linear fixed drug eruption

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Trimethoprim-induced linear fixed drug eruption

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Acquired relapsing self-healing Blaschko dermatitis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Unilateral linear lichenoid eruption after bone marrow transplantation: an unmasking of tolerance to an abnormal keratinocyte clone?

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Somatic mutation and recombination test in Drosophila melanogaster.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Analysis of the relationship between age of larvae at mutagen treatment and frequency and size of spots in the wing somatic mutation and recombination test in Drosophila melanogaster

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Thirty compounds tested in the Drosophila wing spot test.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Antigenotoxicity studies in Drosophila melanogaster.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Hypothesis: vascular twin naevi and somatic recombination in man.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Allelic somatic mutations may explain vascular twin nevi

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

"Cutis tricolor": congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: an unusual example of twin spotting?

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Paired melanotic and achromic macules in a case of phacomatosis pigmentovascularis: a further example of twin spotting?

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Proteus syndrome: an expanded phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Encephalocraniocutaneous lipomatosis and the Proteus syndrome: distinct entities with overlapping manifestations.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Lipomatosis and partial lipohypoplasia in Proteus syndrome: a clinical clue for twin spotting?

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Elattoproteus syndrome: delineation of an inverse form of Proteus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Dominant traits may give rise to paired patches of either excessive or absent involvement

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Phakomatosis pigmentovascularis type IVa

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Phacomatosis pigmentokeratotica: a melanocytic-epidermal twin nevus syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Phacomatosis pigmentokeratotica: a patient with the rare melanocytic-epidermal twin nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Phacomatosis pigmentokeratotica: report of new cases and further delineation of the syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Unilateral dermatomal superficial telangiectasia overlapping Becker's melanosis

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Unilateral eruptive psoriasis and lichen striatus

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Klippel-Trenaunay syndrome: is it a paradominant trait?

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Familial naevus sebaceus may be explained by paradominant transmission

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Becker nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Familial nevus sebaceus

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Familial nevus sebaceus of Jadassohn: occurrence in three generations.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Familial naevus sebaceous of Jadassohn

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Inherited extensive speckled lentiginous nevus with ichthyosis: report of a previously undescribed association

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Genetic aspects of the Klippel-Trenaunay syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

A new case of Klippel-Trenaunay-Weber (KTW) syndrome: evidence of autosomal dominant inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Unilateral dermatomal superficial telangiectasia. Nine new cases and a review of unilateral dermatomal superficial telangiectasia

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Revertant mosaicism in epidermolysis bullosa caused by mitotic gene conversion

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

On the statistical analysis of allelic-loss data

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Genetic mosaicism in normal tissues of Wilms' tumour patients

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

Allelotype analysis of oesophageal adenocarcinoma: loss of heterozygosity occurs at multiple sites

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2899%2970042-3

7 January 2021

10.1016/S0190-9622(99)70042-3

Identifiers

DOI

1 reference

28 July 2017

1 reference