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Corrigendum: Case Report: Prenatal Diagnosis for a Rett Syndrome Family Caused by a Novel MECP2 Deletion With Heteroduplexes of PCR Product.
Zhang, Honghong; Sun, Yixi; Zhu, Yuxia; Hong, Jiali; Zheng, Miaomiao.
Afiliación
  • Zhang H; Department of Pediatrics, Hangzhou Children's Hospital, Hangzhou, China.
  • Sun Y; Department of Reproductive Genetics, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Zhu Y; Key Laboratory of Reproductive Genetics, Ministry of Education, Zhejiang University, Hangzhou, China.
  • Hong J; Department of Pediatrics, Hangzhou Children's Hospital, Hangzhou, China.
  • Zheng M; Department of Pediatrics, Hangzhou Children's Hospital, Hangzhou, China.
Front Pediatr ; 10: 823860, 2022.
Article en En | MEDLINE | ID: mdl-35498794
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Front Pediatr Año: 2022 Tipo del documento: Article País de afiliación: China
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Front Pediatr Año: 2022 Tipo del documento: Article País de afiliación: China