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








Intervalo de ano
1.
Chinese Journal of Medical Genetics ; (6): 267-271, 2009.
Artigo em Chinês | WPRIM | ID: wpr-287410

RESUMO

<p><b>OBJECTIVE</b>To determine the inheritance mode and pathogenesis of a family with brachydactyly type A1 in Jining, Shandong province via clinical feature and disease gene analysis.</p><p><b>METHODS</b>Family survey and clinical examinations were performed to determine the inheritance mode; microsatellite polymorphic markers and polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP)were employed for linkage analysis and mutation screening respectively.</p><p><b>RESULTS</b>The brachydactyly type of the family was type A1 (BDA1), and autosomal dominant inheritance. A missense mutation (G298A) of the indian hedgehog gene (IHH) was identified in the patients of this family.</p><p><b>CONCLUSION</b>A missense mutation G298A of the IHH gene might be the molecular basis for the brachydactyly type A1 in this family from Shandong province.</p>


Assuntos
Feminino , Humanos , Masculino , Sequência de Bases , China , Família , Predisposição Genética para Doença , Genótipo , Proteínas Hedgehog , Genética , Deformidades Congênitas dos Membros , Genética , Mutação , Mutação de Sentido Incorreto , Linhagem , Fenótipo , Polimorfismo de Fragmento de Restrição , Síndrome
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA