Partial trisomy 18 in a family with a translocation (18;21)(q21;q22).

A family is described in which 2 sibs had similar congenital abnormalities. Chromosome investigation of the mother and another child disclosed they were carriers of a translocation t(18;21)(q21;q22). The karyotype of one of the abnormal infants was determined and was found to be consistent with part...

Description complète

Détails bibliographiques

Publié dans:	J Med Genet
Auteurs principaux:	Niazi, M, Coleman, D V, Saldaña-Garcia, P
Format:	Artigo
Langue:	Inglês
Publié:	BMJ Publishing Group 1978
Sujets:	Research Article
Accès en ligne:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1013665/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/641950/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.15.2.148
Tags:	Ajouter un tag Pas de tags, Soyez le premier à ajouter un tag!