Un cas de trisomie 22 incomplète due à la malségrégation méiotique d'une translocation familiale 11:12. [Incomplete trisomy 22 due to meiotic malsegregation of a familial 11:12 translocation.]

Details

Serval ID
serval:BIB_2D61C86FED77
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
Title
Un cas de trisomie 22 incomplète due à la malségrégation méiotique d'une translocation familiale 11:12. [Incomplete trisomy 22 due to meiotic malsegregation of a familial 11:12 translocation.]
Journal
Revue Médicale de la Suisse Romande
Author(s)
Pescia G., Jotterand-Bellomo M., Gaide A.C.
ISSN
0035-3655
Publication state
Published
Issued date
1981
Volume
101
Number
4
Pages
325-359
Language
french
Notes
Publication types: Case Reports ; Journal Article - Publication Status: ppublish
Keywords
Adult, Child, Chromosomes, Human, 21-22 and Y, Dermatoglyphics, Female, Humans, Male, Pedigree, Translocation, Genetic, Trisomy
Pubmed
Create date
22/05/2009 8:37
Last modification date
20/08/2019 13:12
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