A carregar...

Molecular and cytogenetic analysis of a familial microdeletion of Xq.

Cytogenetic analysis of a male infant referred for poor neurological development and failure to thrive showed a microdeletion of the X chromosome, his karyotype being 46,Y,del(X)(pter----q21.1:: q21.2----qter). His mother and grandmother were also found to carry the deletion. DNA probes were used to...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Wells, S, Mould, S, Robins, D, Robinson, D, Jacobs, P
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016798/
https://ncbi.nlm.nih.gov/pubmed/1675684
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!