A carregar...

Evaluation of candidate genes for familial brachydactyly.

Type A1 brachydactyly in humans is a recognisable syndrome characterised by shortening of the middle phalanx of all digits with occasional fusion of the middle and terminal phalanges. The purpose of this study was to evaluate candidate genes for type A1 brachydactyly in two families with multiple af...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Mastrobattista, J M, Dollé, P, Blanton, S H, Northrup, H
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051733/
https://ncbi.nlm.nih.gov/pubmed/8592325
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!