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Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome).
Assia Batzir, Nurit; Posey, Jennifer E; Song, Xiaofei; Akdemir, Zeynep Coban; Rosenfeld, Jill A; Brown, Chester W; Chen, Emily; Holtrop, Shannon G; Mizerik, Elizabeth; Nieto Moreno, Margarita; Payne, Katelyn; Raas-Rothschild, Annick; Scott, Richard; Vernon, Hilary J; Zadeh, Neda; Lupski, James R; Sutton, V Reid.
Afiliação
  • Assia Batzir N; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Posey JE; Texas Children's Hospital, Houston, Texas.
  • Song X; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Akdemir ZC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Brown CW; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Chen E; Le Bonheur Children's Hospital, Memphis, Tennessee.
  • Holtrop SG; Division of Medical Genetics, Department of Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee.
  • Mizerik E; Department of Genetics, Kaiser Permanente, San Francisco, California.
  • Nieto Moreno M; Le Bonheur Children's Hospital, Memphis, Tennessee.
  • Payne K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Raas-Rothschild A; Texas Children's Hospital, Houston, Texas.
  • Scott R; Division of Clinical and Translational Genetics, Dr. John T. Macdonald Foundation Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida.
  • Vernon HJ; Jackson Memorial Hospital, Miami, Florida.
  • Zadeh N; Section of Child Neurology, Department of Neurology, Indiana University School of Medicine, Indianapolis, Indiana.
  • Lupski JR; The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Sutton VR; Clinical Genetics Unit, Great Ormond Street Hospital for Children NHS Trust, London, UK.
Am J Med Genet A ; 182(1): 38-52, 2020 01.
Article em En | MEDLINE | ID: mdl-31782611
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Transposases / Transtornos do Desenvolvimento da Linguagem / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 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 / Transposases / Transtornos do Desenvolvimento da Linguagem / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article