Your browser doesn't support javascript.
loading
Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects.
Chen, Chih-Ping; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Shin-Wen; Wu, Fang-Tzu; Wang, Wayseen.
Afiliação
  • Chen CP; Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health
  • Chern SR; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan.
  • Wu PS; Gene Biodesign Co. Ltd, Taipei, Taiwan.
  • Chen SW; Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan.
  • Wu FT; Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan.
  • Wang W; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan.
Taiwan J Obstet Gynecol ; 60(2): 341-344, 2021 Mar.
Article em En | MEDLINE | ID: mdl-33678339
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Cromossomos Humanos Par 1 / Deficiências do Desenvolvimento / Cardiopatias Congênitas / Deficiência Intelectual Limite: Adolescent / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Cromossomos Humanos Par 1 / Deficiências do Desenvolvimento / Cardiopatias Congênitas / Deficiência Intelectual Limite: Adolescent / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article