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Novel Causative Variants in DYRK1A, KARS, and KAT6A Associated with Intellectual Disability and Additional Phenotypic Features.
Murray, Clark R; Abel, Samantha N; McClure, Matthew B; Foster, Joseph; Walke, Maria I; Jayakar, Parul; Bademci, Guney; Tekin, Mustafa.
Afiliação
  • Murray CR; Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, United States.
  • Abel SN; Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, United States.
  • McClure MB; Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, United States.
  • Foster J; Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, United States.
  • Walke MI; Nicklaus Childreǹs Hospital, Miami, Florida, United States.
  • Jayakar P; Nicklaus Childreǹs Hospital, Miami, Florida, United States.
  • Bademci G; Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, United States.
  • Tekin M; Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, Florida, United States.
J Pediatr Genet ; 6(2): 77-83, 2017 Jun.
Article em En | MEDLINE | ID: mdl-28496994
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Pediatr Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Pediatr Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos