(Q40212424)

18 September 2017

1 reference

title

Dominant susceptibility to cancer in man. (English)

1 reference

18 September 2017

Harnden D

1

1 reference

18 September 2017

Morten J

series ordinal

2

1 reference

18 September 2017

Featherstone T

series ordinal

3

1 reference

18 September 2017

publication date

1 January 1984

1 reference

Advances in Cancer Research

18 September 2017

published in

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18 September 2017

volume

41

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18 September 2017

page(s)

185-255

1 reference

Retinoblastoma - a clinical survey and its genetic implications

18 September 2017

cites work

1 reference

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7 January 2021

Microtubules in retinoblastoma.

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7 January 2021

Eye findings in the 13 trisomy syndrome

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7 January 2021

Linkage analysis of the nevoid basal cell carcinoma syndrome

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7 January 2021

A (13) terminal deletion, 46 chromosomes. Repository identification no. GM-250.

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7 January 2021

Bilateral retinoblastoma with ectopic intracranial retinoblastoma: trilateral retinoblastoma.

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Clonal origin of inherited medullary thyroid carcinoma and pheochromocytoma

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Inherited Medullary Thyroid Carcinoma: A Final Monoclonal Mutation in One of Multiple Clones of Susceptible Cells

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma. A study of 139 cases

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer Gene

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7 January 2021

HL-A antigens in retinoblastoma.

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Epithelioma adenoides cysticum; basal cell nevi, agenesis of the corpus callosum and dental cysts; a clinical and autopsy study

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Management of Parathyroid Glands in Surgery for Medullary Thyroid Carcinoma

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

A possible relationship of neuroblastoma to von recklinghausen's disease

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Excess of cancer deaths in grandparents of patients with retinoblastoma.

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Segregation analysis in hereditary retinoblastoma

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Associated congenital malformations in retinoblastoma

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Mutation theory of carcinogenesis in retinoblastoma

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Topical chemotherapy of dysplastic melanocytic nevi with 5% fluorouracil

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Von Recklinghausen's disease: a clinicopathological study.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

An unusual pedigree with retinoblastoma. Does it shed light on the delayed mutation and host resistance theories?

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Malignant transformation of human embryo retinoblasts by cloned adenovirus 12 DNA

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https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Mutational mosaicism and genetic counseling in retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Adrenal medullary disease in multiple endocrine neoplasia, type 2: pheochromocytoma and its precursors

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Chromosome aberrations and radiation-induced cell death. I. Transmission and survival parameters of aberrations

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

A New Familial Cancer Syndrome? A Spectrum of Malignant and Benign Tumors Including Retinoblastoma, Carcinoma of the Bladder and Other Genitourinary Tumors, Thyroid Adenoma, and a Probable Case of Multifocal Osteosarcoma2

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

An autosomal dominant inheritance for multiple sunlight-induced malignancy in a patient without abnormalities in DNA repair or replication. Repository identification No. GM2881.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Radiosensitivity in cultured human fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Increased tetraploidy: cell-specific for the Gardner gene in the cultured cell

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Increased in vitro tetraploidy: tissue specific within the heritable colorectal cancer syndromes with polyposis coli.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

In vitro studies on adenomatosis of the colon and rectum

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Tetraploid fibroblasts and familial polyposis coli

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Proliferative patterns in colonic mucosa in familial polyposis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Possible inactivation of part of chromosome 13 due to 13qXp translocation associated with retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Radiosensitivity of fibroblasts from patients with retinoblastoma and chromosome-13 anomalies

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Dysplastic nevus syndrome: a phenotypic association of sporadic cutaneous melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Inherited gastrointestinal-polyposis syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

SCE and UDS studies in a family with retinoblastoma: A case study

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Multiple Cell Origin of Hereditary Neurofibromas

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Skin cancer in black patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma and Osteogenic Sarcoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma: analysis of 235 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoma: spontaneous regression of retinoblastoma or benign manifestation of the mutation?

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Numerical and structural chromosome aberrations in cultured lymphocytes and cutaneous fibroblasts of patients with multiple adenomas of the colorectum

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Multiple karyotypic changes in retinoblastoma tumor cells: Presence of normal chromosome No. 13 in most tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Identification of a cell-surface antigen selectively expressed on the natural killer cell

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Pheochromocytoma; its relationship to the neurocutaneous syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Basal cell carcinomas following roentgen therapy of ankylosing spondylitis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Pathogenesis of colonic polyps in multiple juvenile polyposis:Report of a case associated with gastric polyps and carcinoma of the rectum

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

MULTIPLE BASAL-CELL NEVI SYNDROME. AN ANALYSIS OF A SYNDROME CONSISTING OF MULTIPLE NEVOID BASAL-CELL CARCINOMA, JAW CYSTS, SKELETAL ANOMALIES, MEDULLOBLASTOMA, AND HYPORESPONSIVENESS TO PARATHORMONE.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

THE GENETICS OF RETINOBLASTOMA.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

A method for the scrutiny of live mammalian cells in culture and for the measurement of their proliferative ability after x-irradiation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Cytogenetically marked clones in human fibroblasts cultured from normal subjects

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Skin cancer in Sunny Queensland

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma A Model of Hereditary Fragile Chromosomal Regions

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

In vitro growth characteristics of skin fibroblasts from patients with adenomatosis of the colon and rectum and their relatives

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The cytological differentiating potential of pineal parenchymal neoplasms (true pinealomas). A clinicopathological study of 28 tumours

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Model for the incidence of embryonal cancers: application to retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Two-step mutation theory for retinoblastoma: ultrastructural support

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Gastrointestinal involvement in von Recklinghausen's neurofibromatosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Multiple Palmar Basal Cell Epitheliomas in Basal Cell Nevus Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Chromosome 14q+ in a retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Transformation of epithelioma adenoides cysticum into multiple rodent ulcers: fact or fallacy. A historical vignette

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The basal-cell nevus: its relationship to multiple cutaneous cancers and associated anomalies of development

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma: epidemiologic characteristics

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma and its association with a deletion in chromosome #13: a survey using high-resolution chromosome techniques.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Basal Cell Nevus Syndrome Associated with Malignant Melanoma of the Iris

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Nevoid basal-cell carcinoma syndrome. Report of two cases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Absence of chromosome breakage in patients with retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Mutation and cancer: statistical study of retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Developmental Genetics of Neuroblastoma12

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Human skin fibroblasts from individuals genetically predisposed to cancer are sensitive to an SV40-induced T antigen display and transformation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Tumour promoter alone induces neoplastic transformation of fibroblasts from humans genetically predisposed to cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Organization of actin‐containing cables in cultured skin fibroblasts from individuals at high risk of colon cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Fibroblasts from Retinoblastoma patients: Enhanced growth in fetal calf serum and a normal response to ionizing radiation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Cell culture studies on neurofibromatosis (von Recklinghausen). I. Comparative growth experiments with fibroblasts at high and low concentrations of fetal calf serum

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Risk of second tumors in survivors of childhood cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

High uric acid and urea clearance in cirrhosis secondary to increased "effective vascular volume"

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Abnormal sensitivity of diploid skin fibroblasts from a family with gardner's syndrome to the lethal effects of X-irradiation, ultraviolet light and mitomycin-C

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Familial basal cell nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Hl-a in cancer family “n”

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Role of heredity in multiple primary cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Familial atypical multiple mole-melanoma syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Familial atypical multiple mole melanoma (FAMMM) syndrome: genetic heterogeneity and malignant melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Phenotypic variation in the familial atypical multiple mole-melanoma syndrome (FAMMM)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Inheritance of Retinoblastoma in Ohio

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Adenovirus-12 genes undetectable in human retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Radiation-induced skin cancer of the head and neck

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Tritiated thymidine incorporation into epithelial cells of normal-appearing colorectal mucosa of cancer patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Hereditary retinoblastoma: penetrance, expressivity and age of onset

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma: mutational mosaicism or host resistance?

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Multiple nevoid basal cell carcinoma syndrome: radiological manifestations

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

MULTIPLE PRIMORDIAL CYSTS ASSOCIATED WITH BIFID RIB AND OCULAR DEFECTS

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Deletion of 13q in two patients with retinoblastoma, one probably due to 13q- mosaicism in the mother

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Gorlin's syndrome. A radiological and cytogenetic study of nine cases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Chromosome banding pattern in human colonic polyps

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Susceptibility of skin fibroblasts from patients with retinoblastoma to transformation by murine sarcoma virus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Family studies on the chromosomal location of the retinoblastoma gene (Rb-1).

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Lymphocyte chromosome survey in 42 patients with retinoblastoma: Effort to detect 13q14 deletion mosaicism

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma in a boy with a de novo mutation of a 13/18 translocation: the assumption that the retinoblastoma locus is at 13q141, particularly at the distal portion of it

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinal Tumor Induction by Ocular Inoculation of Human Adenovirus in 3-Day-Old Rats

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma-like neoplasm induced in C3H/BifB/Ki strain mice by human adenovirus serotype 12.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinal tumor induced in the baboon by human adenovirus 12.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Mitosis in the Nontumorous parts of the Retina with Retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Neurological involvement in the nevoid basal cell carcinoma syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Somatic variation and multiple neurofibromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Further observations on a 13qXp translocation associated with retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Partial deletions and trisomies of chromosome 13; Mapping of bands associated with particular malformations

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Radiological aspects of the basal cell naevus syndrome (Gorlin-Goltz syndrome) (author's transl)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma, chromosome 13, and in vitro cellular radiosensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The histogenesis of retinoblastoma. An electron-microscopic analysis of rosette

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Malignancy and Transformation: Expression in Somatic Cell Hybrids and Variants

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Chiasma derived genetic maps and recombination fractions: chromosome 13 with reference to the proposed 13q14 retinoblastoma locus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Impaired colony-forming ability following gamma irradiation of skin fibroblasts from tuberous sclerosis patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Familial renal cell carcinoma with a 3;11 chromosome translocation limited to tumor cells

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma: An epidemiological study (survey and review)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Differential genetic susceptibility of cultured human skin fibroblasts to transformation by Kirsten murine sarcoma virus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Growth abnormalities of cultured human skin fibroblasts derived from individuals with hereditary adenomatosis of the colon and rectum

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

HEREDITARY CUTANEMOMANDIBULAR POLYONCOSIS. A SYNDROME OF MYRIAD BASAL-CELL NEVI OF THE SKIN, MANDIBULAR CYSTS, AND INCONSTANT SKELETAL ANOMALIES.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Basal cell nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The use of multiple thresholds in determining the mode of transmission of semi-continuous traits.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Characteristics of an established cell line of retinoblastoma.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Chemical transformation of cultured human skin fibroblasts derived from individuals with hereditary adenomatosis of the colon and rectum.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Decreased UV-induced DNA repair synthesis in peripheral leukocytes from patients with the nevoid basal cell carcinoma syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma-del(13q14): Report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Genetic mapping of a murine leukemia virus-inducing locus of AKR mice

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Familial juvenile colonic polyposis with associated colon cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The multiple basal-cell nevus syndrome in a Negro family

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Radiation induced neoplasia following external beam therapy for children with retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The heredity of retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Increased nerve-growth-stimulating activity in disseminated neurofibromatosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Interstitial deletion 13q syndromes: a report on two unrelated patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Abnormal sensitivity to UV-radiation in cultured skin fibroblasts from patients with hereditary cutaneous malignant melanoma and dysplastic nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Radiation-induced neoplasms following curative therapy for retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The basal cell nevus syndrome.Disasters occurring among a series of 36 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Pinealoblastoma with retinoblastomatous differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Familial Retinoblastoma and Chromosome 13 Deletion Transmitted via an Insertional Translocation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

A possible population monitoring system on environmental mutagens: Statistical studies on retinoblastoma in Japan

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Retinoblastoma in Finland 1912-1964

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The evidence for a retinoblastoma induction factor

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The multiple nevoid basal cell carcinoma syndrome. Report of its occurrence in four generations of a family

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Peutz-Jeghers syndrome and bilateral breast carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The Nature of Retinoblastoma. Ii. Photoreceptor Differentiation: An Electron Microscopic Study

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

The electroencephalogram (EEG) as a research tool in human behavior genetics: psychological examinations in healthy males with various inherited EEG variants. I. Rationale of the study. Material. Methods. Heritability of test parameters

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Naevoid basal celled carcinoma associated with a dyskeratosis of the palms and soles. A new entity.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

In vitro radiosensitivity of human dipliod fibroblasts derived from patients with unusual clinical responses to radiation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Skin fibroblasts from a D-deletion type retinoblastoma patient are abnormally X-ray sensitive

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

X-ray sensitivity of diploid fibroblasts from patients with hereditary or sporadic retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

New Findings in the Chromosome 13 Long-Arm Deletion Syndrome and Retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Genetic aspects of adenomatosis of endocrine glands

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Chromosomal anomalies in patients with retinoblastoma.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

C-Cell Hyperplasia Preceding Medullary Thyroid Carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Normal repair of gamma radiation-induced single-strand and double-strand DNA breaks in retinoblastoma fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Bilateral Acoustic Neuroma in a Large Kindred

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Trisomy for the distal end of the short arm of chromosome 3: a syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

Cell death, chromosome damage and mitotic delay in normal human, ataxia telangiectasia and retinoblastoma fibroblasts after x-irradiation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2808%2960017-2

7 January 2021

10.1016/S0065-230X(08)60017-2

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