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De novo 2q36.3q37.1 deletion encompassing TRIP12 and NPPC yields distinct phenotypes.
Kondo, Yuto; Aoyama, Kohei; Suzuki, Hisato; Hattori, Ayako; Hori, Ikumi; Ito, Koichi; Yoshida, Aya; Koroki, Mari; Ueda, Kentaro; Kosaki, Kenjiro; Saitoh, Shinji.
Afiliación
  • Kondo Y; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Aoyama K; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Suzuki H; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
  • Hattori A; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Hori I; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Ito K; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Yoshida A; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Koroki M; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Ueda K; Department of Pediatrics, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan.
  • Kosaki K; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Saitoh S; Department of Pediatrics, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan.
Hum Genome Var ; 7: 19, 2020.
Article en En | MEDLINE | ID: mdl-32528716
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Hum Genome Var Año: 2020 Tipo del documento: Article País de afiliación: Japón
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Hum Genome Var Año: 2020 Tipo del documento: Article País de afiliación: Japón