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Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning Algorithm.
Callaway, Danielle A; Campbell, Ian M; Stover, Samantha R; Hernandez-Garcia, Andres; Jhangiani, Shalini N; Punetha, Jaya; Paine, Ingrid S; Posey, Jennifer E; Muzny, Donna; Lally, Kevin P; Lupski, James R; Shaw, Chad A; Fernandes, Caraciolo J; Scott, Daryl A.
Afiliación
  • Callaway DA; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, United States.
  • Campbell IM; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States.
  • Stover SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States.
  • Hernandez-Garcia A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States.
  • Jhangiani SN; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States.
  • Punetha J; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States.
  • Paine IS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States.
  • Posey JE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States.
  • Muzny D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States.
  • Lally KP; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States.
  • Lupski JR; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States.
  • Shaw CA; Department of Pediatric Surgery, McGovern Medical School at UT Health, Houston, Texas, United States.
  • Fernandes CJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States.
  • Scott DA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States.
J Pediatr Genet ; 7(4): 164-173, 2018 Dec.
Article en En | MEDLINE | ID: mdl-30430034
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Pediatr Genet Año: 2018 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Pediatr Genet Año: 2018 Tipo del documento: Article