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Impact of genetic subtypes of Prader-Willi syndrome with growth hormone therapy on intelligence and body mass index.
Butler, Merlin G; Matthews, Naomi A; Patel, Nidhi; Surampalli, Abhilasha; Gold, June-Anne; Khare, Manaswitha; Thompson, Travis; Cassidy, Suzanne B; Kimonis, Virginia E.
Afiliación
  • Butler MG; Division of Research and Genetics, Department of Psychiatry and Behavioral Sciences, University of Kansas Medical Center, Kansas City, Kansas.
  • Matthews NA; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California.
  • Patel N; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California.
  • Surampalli A; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California.
  • Gold JA; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California.
  • Khare M; Division of Genetics and Metabolism, Department of Pediatrics, University of Loma Linda, Loma Linda, California.
  • Thompson T; Children's Hospital of Orange County, Orange, California.
  • Cassidy SB; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine, California.
  • Kimonis VE; Department of Educational Psychology, University of Minnesota, Twin Cities, Minnesota.
Am J Med Genet A ; 179(9): 1826-1835, 2019 09.
Article en En | MEDLINE | ID: mdl-31313492
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Cromosomas Humanos Par 15 / Hormona del Crecimiento / Eliminación de Secuencia Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Imprimir
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PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Cromosomas Humanos Par 15 / Hormona del Crecimiento / Eliminación de Secuencia Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos