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PMID: 7447607 Published · ppublish fre Case Reports English Abstract Journal Article

[Retinoblastoma and interstitial deletion of 13q (author's transl)].

Rétinoblastome et délétion intercalaire du chromosome 13.

Archives francaises de pediatrie ·Vol. 37 ·No. 8 ·1980-10-00 ·Pages 531-5

De Grouchy J, Turleau C, Cabanis MO, Richardet JM

Abstract

The authors report an observation of retinoblastoma associated with partial monosomy 13q [46, XY, t (2;10) (q21;q24), inv(9), del(13)(q13q213)] and discuss the origin of this exceptional childhood tumor by gene mutation of chromosome rearrangement.

MeSH Terms
Child Child, Preschool Chromosome Deletion Chromosomes, Human, 13-15 Eye Neoplasms/genetics Female Humans Infant Infant, Newborn Male Phenotype Retinoblastoma/genetics
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
De Grouchy J
Turleau C
Cabanis M O
Richardet J M
Article Info
Journal
Archives francaises de pediatrie
Abbr.
Arch Fr Pediatr
ISSN
0003-9764
Published
1980-10-00
Pages
531-5
Language
fre
Region
France
NLM ID
0372421
Subset
IM
External Links
PubMed source
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