Home LiteratureArticle Details
PMID: 6823558 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

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

Science (New York, N.Y.) ·Vol. 219 ·No. 4587 ·1983-02-25 ·Pages 971-3

Sparkes RS, Murphree AL, Lingua RW, Sparkes MC, Field LL, Funderburk SJ, Benedict WF

Abstract

Evaluation of three families with hereditary retinoblastoma demonstrates close linkage of the gene for this tumor with the genetic locus for esterase D. These results assign the gene for the hereditary form of retinoblastoma to band q14 on chromosome 13, the same region which is affected in the chromosome deletion form of this eye tumor, and therefore suggest a common underlying mechanism in the pathogenesis of these two forms of retinoblastoma.

MeSH Terms
Chromosome Deletion Chromosome Mapping Chromosomes, Human, 13-15 Esterases/genetics Genetic Linkage Humans Retinoblastoma/genetics
Chemicals
Esterases
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Sparkes R S
Murphree A L
Lingua R W
Sparkes M C
Field L L
Funderburk S J
Benedict W F
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1983-02-25
Pages
971-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NEI NIH HHS · EY-02715 · United States
NICHD NIH HHS · HD-04612 · United States
NICHD NIH HHS · HD-05615 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]