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Brachydactyly type A3 is caused by a novel 13 bp HOXD13 frameshift deletion in a Chinese family.
Zhang, Mengshu; Lu, Likui; Wei, Bin; Zhang, Yingying; Li, Xiang; Shi, Yajun; Ge, Wei; Sun, Miao.
Afiliación
  • Zhang M; Institute for Fetology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Lu L; Institute for Fetology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Wei B; Institute for Fetology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Zhang Y; Institute for Fetology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Li X; Institute for Fetology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Shi Y; Institute for Fetology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
  • Ge W; Department of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Sun M; Institute for Fetology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Am J Med Genet A ; 182(10): 2432-2436, 2020 10.
Article en En | MEDLINE | ID: mdl-32789964
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Sindactilia / Proteínas de Homeodominio / Predisposición Genética a la Enfermedad / Braquidactilia Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Sindactilia / Proteínas de Homeodominio / Predisposición Genética a la Enfermedad / Braquidactilia Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article