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.]
| Data(s) |
1981
|
|---|---|
| Identificador |
http://serval.unil.ch/?id=serval:BIB_2D61C86FED77 isbn:0035-3655 pmid:7256062 |
| Idioma(s) |
fr |
| Fonte |
Revue Médicale de la Suisse Romande, vol. 101, no. 4, pp. 325-359 |
| Palavras-Chave | #Adult; Child; Chromosomes, Human, 21-22 and Y; Dermatoglyphics; Female; Humans; Male; Pedigree; Translocation, Genetic; Trisomy |
| Tipo |
info:eu-repo/semantics/article article |
