Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Am J Med Genet ; 21(3): 439-44, 1985 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-3895927

RESUMO

A fetus with Weyers oligodactyly was studied after a previous sibling had been born with that condition. Prenatal diagnosis was undertaken using ultrasound to visualize the long bones, which were found to be severely affected by the condition at 19 weeks of gestation. Most notable were the ulnae and fibulae, which were very short; the fetus had bilateral hydronephrosis.


Assuntos
Fíbula/anormalidades , Dedos/anormalidades , Genes Recessivos , Hidronefrose/genética , Diagnóstico Pré-Natal , Dedos do Pé/anormalidades , Ulna/anormalidades , Ultrassonografia , Adulto , Feminino , Humanos , Hidronefrose/diagnóstico , Masculino , Gravidez , Síndrome
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...