(Q35194574)

English

Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s) (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

plexiform neurofibroma

1 reference

based on heuristic

inferred from title

author name string

E M Petty

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

L H Gibson

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

J W Fountain

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

J L Bolognia

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

T L Yang-Feng

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

D E Housman

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

A E Bale

7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

language of work or name

0 references

publication date

1 July 1993

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

American Journal of Human Genetics

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

53

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

96-104

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Mutation and cancer: statistical study of retinoblastoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

A rapid method for the purification of DNA from blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Homozygous deletion of the alpha- and beta 1-interferon genes in human leukemia and derived cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Genetic aspects of cutaneous malignant melanoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome Ip36.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Absence of IFNA and IFNB genes from human malignant glioma cell lines and lack of correlation with cellular sensitivity to interferons.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

A genetic model for colorectal tumorigenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Cancer statistics, 1990.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Malignant melanoma in the 1990s: the continued importance of early detection and the role of physician examination and self-examination of the skin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Chromosome 9 deletion mapping reveals interferon alpha and interferon beta-1 gene deletions in human glial tumors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Human malignant melanoma significance of chromosomal abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Exclusion of the familial melanoma locus (MLM) from the PND/D1S47 and MYCL1 regions of chromosome arm 1p in 7 Australian pedigrees.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Homozygous deletions within human chromosome band 9p21 in melanoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Genetic and physical map of the interferon region on chromosome 9p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Familial atypical multiple mole-melanoma syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

A pericentric inversion of chromosome 9 and a rearrangement involving chromosomes 9 and 10, observed in two generations. Clinical description of chromosome 9 (p12-p21) deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682234

28 July 2018

Deletion 9p, duplication 18q in two sisters resulting from a maternal (9;18) (p22;q21.3) translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal evolution in the progression and metastasis of human malignant melanoma. A multiple lesion study

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary melanoma in Australia variable association with dysplastic nevi and

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetics of non-small cell lung cancer: analysis of consistent non-random abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic Analysis Workshop 7: Summary of the melanoma workshop

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage map of human chromosome 9 microsatellite polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cutaneous malignant melanoma and atypical moles associated with a constitutional rearrangement of chromosomes 5 and 9

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New cutaneous phenotype in familial malignant melanoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High risk of malignant melanoma in melanoma-prone families with dysplastic nevi

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Karyotypic evolution in human malignant melanoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The rate of malignant melanoma in the United States: are we making an impact?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis of melanocytes from premalignant nevi and melanomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HMB-45 staining of dysplastic nevi. Support for a spectrum of progression toward melanoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8317504

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8317504%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q35194574&oldid=1526770806"