Your browser doesn't support javascript.
loading
Expanding the reproductive organ phenotype of CHD7-spectrum disorder.
Nomakuchi, Tomoki T; Danowitz, Melinda; Stewart, Blythe; Leonard, Jacqueline; Izumi, Kosuke; Krantz, Ian; Kolon, Thomas F; Langdon, David; Skraban, Cara; Van Batavia, Jason; Zackai, Elaine; Jiao, Kai; Linn, Rebecca; Alexander, Caitlin; Zaontz, Mark; Vogiatzi, Maria G; Pyle, Louise C.
Afiliación
  • Nomakuchi TT; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Danowitz M; Division of Endocrinology, Children's Hospital of Philadelphia, Philadelphia, USA.
  • Stewart B; Human Genetics Unit, University of Edinburgh, Edinburgh, Scotland, United Kingdom.
  • Leonard J; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Izumi K; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Krantz I; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Kolon TF; Division of Urology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Langdon D; Division of Endocrinology, Children's Hospital of Philadelphia, Philadelphia, USA.
  • Skraban C; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Van Batavia J; Division of Urology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Zackai E; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Jiao K; Center for Biotechnology & Genomic Medicine, Medical College of Georgia at Augusta University, Augusta, GA, USA.
  • Linn R; Division of Pathology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Alexander C; Division of Pathology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Zaontz M; Division of Urology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Vogiatzi MG; Division of Endocrinology, Children's Hospital of Philadelphia, Philadelphia, USA.
  • Pyle LC; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Am J Med Genet A ; 191(5): 1418-1424, 2023 05.
Article en En | MEDLINE | ID: mdl-36794641
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos del Desarrollo Sexual / Criptorquidismo / Síndrome CHARGE Límite: Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos del Desarrollo Sexual / Criptorquidismo / Síndrome CHARGE Límite: Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos