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PMID: 730167 Published · ppublish fre Case Reports English Abstract Journal Article

[A case of bilateral retinoblastoma with monosomy 13 (q12 leads to 114) (author's transl)].

Un cas de rétinoblastome bilatéral avec monosomie 13 partielle (q12 leads to q14).

Human genetics ·Vol. 44 ·No. 2 ·1978-10-31 ·Pages 219-26

Walbaum R, François P, Farriaux JP, Woillez M

Abstract

A partial monosomy 13 by interstitial deletion was found in the complement of a girl with mild mental retardation and bilateral retinoblastoma. Break points were at 13q12 and 13q14. After comparison with other known observations of retinoblastoma with deletion of chromosome 13, it is suggested that the deletion common to these patients may be band 13q14. The most likely pathogenic hypothesis seems to be the haplo-insufficiency.

MeSH Terms
Child, Preschool Chromosome Deletion Chromosomes, Human/ultrastructure Chromosomes, Human, 13-15 Dermatoglyphics Eye Neoplasms/genetics Female Humans Intellectual Disability/genetics Karyotyping Retinoblastoma/genetics
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Walbaum R
François P
Farriaux J P
Woillez M
References (24)
24 references, click to expand
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Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1978-10-31
Pages
219-26
Language
fre
Region
Germany
NLM ID
7613873
Subset
IM
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