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FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?
Myers, Angela; du Souich, Christèle; Yang, Connie L; Borovik, Lior; Mwenifumbo, Jill; Rupps, Rosemarie; Study, Causes; Lehman, Anna; Boerkoel, Cornelius F.
Afiliação
  • Myers A; Department of Pediatrics, University of South Dakota and Sanford Health, Sioux Falls, South Dakota.
  • du Souich C; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Yang CL; BC Children's Hospital Research Institute, Children's and Women's Health Centre of British Columbia, Vancouver, British Columbia, Canada.
  • Borovik L; Division of Respiratory Medicine, Department of Pediatrics, University of British Columbia, and Children's and Women's Health Centre of British Columbia, Vancouver, British Columbia, Canada.
  • Mwenifumbo J; Department of Genetic Counseling, Sanford Health, Sioux Falls, South Dakota.
  • Rupps R; BC Children's Hospital Research Institute, Children's and Women's Health Centre of British Columbia, Vancouver, British Columbia, Canada.
  • Study C; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Lehman A; BC Children's Hospital Research Institute, Children's and Women's Health Centre of British Columbia, Vancouver, British Columbia, Canada.
  • Boerkoel CF; BC Children's Hospital Research Institute, Children's and Women's Health Centre of British Columbia, Vancouver, British Columbia, Canada.
Am J Med Genet A ; 173(12): 3172-3181, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28884888
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Fatores de Transcrição Forkhead / Transtorno do Espectro Autista / Transtornos da Linguagem / Pneumopatias / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 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: Proteínas Repressoras / Fatores de Transcrição Forkhead / Transtorno do Espectro Autista / Transtornos da Linguagem / Pneumopatias / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article