A carregar...

The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome.

A case is reported where the major clinical features of craniostenosis and radial aplasia led to an initial diagnosis of Baller-Gerold syndrome. Mild fibular hypoplasia on skeletal survey led to review of the diagnosis and the similarity of the facial phenotype to that of Roberts syndrome was noted....

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Huson, S M, Rodgers, C S, Hall, C M, Winter, R M
Formato: Artigo
Idioma:Inglês
Publicado em: 1990
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1017134/
https://ncbi.nlm.nih.gov/pubmed/2359099
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!