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"Liu-Liang-Chung" syndrome with multiple congenital anomalies and the distinctive craniofacial features caused by dominant ZEB2 gene gain mutation.
Liu, Wei-Liang; Li, Fang; Chen, Wei; Liu, Lu; Cheng, Hai-Jian; He, Zhi-Xu; Ai, Rong.
Afiliación
  • Liu WL; Department of Pediatrics, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China. liuweiliang205@aliyun.com.
  • Li F; Department of Ophthalmology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.
  • Chen W; Department of Ophthalmology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.
  • Liu L; Department of Ophthalmology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.
  • Cheng HJ; Beijing Kangso Medical Laboratory Co., Ltd, Beijing, 100195, China.
  • He ZX; Department of Pediatrics, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.
  • Ai R; Department of Pediatrics, Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.
BMC Pediatr ; 23(1): 480, 2023 09 21.
Article en En | MEDLINE | ID: mdl-37735378
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Enfermedad de Hirschsprung Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2023 Tipo del documento: Article País de afiliación: China
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Enfermedad de Hirschsprung Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2023 Tipo del documento: Article País de afiliación: China