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Functional genomics analysis of Phelan-McDermid syndrome 22q13 region during human neurodevelopment.
Ziats, Catherine A; Grosvenor, Luke P; Sarasua, Sara M; Thurm, Audrey E; Swedo, Susan E; Mahfouz, Ahmed; Rennert, Owen M; Ziats, Mark N.
Afiliação
  • Ziats CA; Division of Intramural Research, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Grosvenor LP; Pediatrics and Developmental Neuroscience Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Sarasua SM; Simons Foundation Autism Research Initiative, New York, New York, United States of America.
  • Thurm AE; School of Nursing, Clemson University, Clemson, South Carolina, United States of America.
  • Swedo SE; Pediatrics and Developmental Neuroscience Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Mahfouz A; Pediatrics and Developmental Neuroscience Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Rennert OM; Delft Bioinformatics Lab, Delft University of Technology, Delft, The Netherlands.
  • Ziats MN; Division of Intramural Research, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS One ; 14(3): e0213921, 2019.
Article em En | MEDLINE | ID: mdl-30875393
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Cromossômicos Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Cromossômicos Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos