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PMID: 3365680 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

Bilateral retinoblastoma associated with 13q-mosaicism. Possible manifestation of a germinal mutation.

Cancer genetics and cytogenetics ·Vol. 32 ·No. 2 ·1988-06-00 ·Pages 169-75

Ribeiro MC, Andrade JA, Erwenne CM, Brunoni D

Abstract

Fifteen retinoblastoma patients were studied cytogenetically using G- and R-banding techniques. One patient showed 13q-mosaicism. It is suggested that a postzygotic deficiency in mosaic cases and in tumoral cells may be secondary to germinal mutation.

MeSH Terms
Child, Preschool Chromosome Banding Chromosome Deletion Chromosomes, Human, Pair 13 Eye Neoplasms/genetics,pathology Female Humans Infant Karyotyping Male Mosaicism Mutation Retinoblastoma/genetics,pathology
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ribeiro M C
Disciplina de Genética da Escola Paulista de Medicina, São Paulo, Brazil.
Andrade J A
Erwenne C M
Brunoni D
Article Info
Journal
Cancer genetics and cytogenetics
Abbr.
Cancer Genet Cytogenet
ISSN
0165-4608
DOI
10.1016/0165-4608(88)90279-8
Published
1988-06-00
Pages
169-75
Language
English
Region
United States
NLM ID
7909240
Subset
IM
External Links
PubMed source DOI: 10.1016/0165-4608(88)90279-8 View journal details
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