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PMID: 1086628 Published · ppublish fre Case Reports English Abstract Journal Article

[2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].

Deux cas de trisomie 10p partielle dus à une translocation paternelle t(10;18)(p13;q23

Annales de genetique ·Vol. 19 ·No. 3 ·1976-09-00 ·Pages 195-7

Morić-Petrović S, Laća Z, Krajgher A, Milośevic J

Abstract

Two brothers trisomic for the distal two thirds of 10p are reported. Trisomy results from the malsegregation of a familial translocation rcp (10;18)(p13;q23) present in the father, a half-brother and the grand-father of the propositi. The phenotype is comparable to that of other 10p trisomic patients reported in the literature.

MeSH Terms

Child, Preschool Chromosome Aberrations/genetics Chromosome Disorders Chromosomes, Human, 16-18 Chromosomes, Human, 6-12 and X Humans Male Translocation, Genetic Trisomy

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Morić-Petrović S

Laća Z

Krajgher A

Milośevic J

Article Info

Journal

Annales de genetique

Abbr.

Ann Genet

ISSN

0003-3995

Published

1976-09-00

Pages

195-7

Language

fre

Region

Netherlands

NLM ID

0370562

Subset

External Links

PubMed source

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[2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].

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