Your browser doesn't support javascript.
loading
Novel MNX1 mutations and genotype-phenotype analysis of patients with Currarino syndrome.
Han, Lu; Zhang, Zhen; Wang, Hui; Song, Hui; Gao, Qing; Yan, Yuchun; Tao, Ran; Xiao, Ping; Li, Long; Jiang, Qian; Li, Qi.
Afiliación
  • Han L; Department of Medical Genetics, Capital Institute of Pediatrics, No. 2 Yabao Rd., Chaoyang District, Beijing, 100020, China.
  • Zhang Z; Department of General Surgery, Capital Institute of Pediatrics Affiliated Children's Hospital, No. 2 Yabao Rd., Chaoyang District, Beijing, 100020, China.
  • Wang H; Department of Medical Genetics, Capital Institute of Pediatrics, No. 2 Yabao Rd., Chaoyang District, Beijing, 100020, China.
  • Song H; Department of General Surgery, Capital Institute of Pediatrics Affiliated Children's Hospital, No. 2 Yabao Rd., Chaoyang District, Beijing, 100020, China.
  • Gao Q; Department of General Surgery, Capital Institute of Pediatrics Affiliated Children's Hospital, No. 2 Yabao Rd., Chaoyang District, Beijing, 100020, China.
  • Yan Y; Department of Radiology, Capital Institute of Pediatrics Affiliated Children's Hospital, Beijing, 100020, China.
  • Tao R; Department of Radiology, Capital Institute of Pediatrics Affiliated Children's Hospital, Beijing, 100020, China.
  • Xiao P; Department of Pathology, Capital Institute of Pediatrics Affiliated Children's Hospital, Beijing, 100020, China.
  • Li L; Department of General Surgery, Capital Institute of Pediatrics Affiliated Children's Hospital, No. 2 Yabao Rd., Chaoyang District, Beijing, 100020, China.
  • Jiang Q; Department of Medical Genetics, Capital Institute of Pediatrics, No. 2 Yabao Rd., Chaoyang District, Beijing, 100020, China. teaco@126.com.
  • Li Q; Department of General Surgery, Capital Institute of Pediatrics Affiliated Children's Hospital, No. 2 Yabao Rd., Chaoyang District, Beijing, 100020, China. l817@sina.com.
Orphanet J Rare Dis ; 15(1): 155, 2020 06 22.
Article en En | MEDLINE | ID: mdl-32571425
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Proteínas de Homeodominio Tipo de estudio: Prognostic_studies Límite: Child / Humans País/Región como asunto: Asia Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: China
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Proteínas de Homeodominio Tipo de estudio: Prognostic_studies Límite: Child / Humans País/Región como asunto: Asia Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: China