Your browser doesn't support javascript.
loading
[A case of a syndrome characterized by short stature, and developmental delay caused by heterozygous variation in the FOXP4 gene].
Ding, S Y; Zhang, Q W; Guo, D F; Feng, B; Zheng, H; Lu, X P.
Afiliação
  • Ding SY; Pediatric Hospital of the First Affiliated Hospital of Henan University of Chinese Medicine College of Pediatrics Henan University of Chinese Medicine, Zhengzhou 450000, China.
  • Zhang QW; Pediatric Hospital of the First Affiliated Hospital of Henan University of Chinese Medicine College of Pediatrics Henan University of Chinese Medicine, Zhengzhou 450000, China.
  • Guo DF; Pediatric Hospital of the First Affiliated Hospital of Henan University of Chinese Medicine College of Pediatrics Henan University of Chinese Medicine, Zhengzhou 450000, China.
  • Feng B; Pediatric Hospital of the First Affiliated Hospital of Henan University of Chinese Medicine College of Pediatrics Henan University of Chinese Medicine, Zhengzhou 450000, China.
  • Zheng H; Pediatric Hospital of the First Affiliated Hospital of Henan University of Chinese Medicine College of Pediatrics Henan University of Chinese Medicine, Zhengzhou 450000, China.
  • Lu XP; Pediatric Hospital of the First Affiliated Hospital of Henan University of Chinese Medicine College of Pediatrics Henan University of Chinese Medicine, Zhengzhou 450000, China.
Zhonghua Er Ke Za Zhi ; 62(6): 571-573, 2024 Jun 02.
Article em Zh | MEDLINE | ID: mdl-38763881
Assuntos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Fatores de Transcrição Forkhead / Heterozigoto Limite: Child / Humans / Male Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: China
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Fatores de Transcrição Forkhead / Heterozigoto Limite: Child / Humans / Male Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: China