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Clinical utility of exome sequencing in infantile heart failure.
Ritter, Alyssa; Bedoukian, Emma; Berger, Justin H; Copenheaver, Deborah; Gray, Christopher; Krantz, Ian; Izumi, Kosuke; Juusola, Jane; Leonard, Jacqueline; Lin, Kimberly; Medne, Livija; Santani, Avni; Skraban, Cara; Yang, Sandra; Ahrens-Nicklas, Rebecca C.
Affiliation
  • Ritter A; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Bedoukian E; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Berger JH; Individualized Medical Genetic Center, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Copenheaver D; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Gray C; GeneDx, Inc, Gaithersburg, MD, USA.
  • Krantz I; Individualized Medical Genetic Center, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Izumi K; Individualized Medical Genetic Center, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Juusola J; Individualized Medical Genetic Center, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Leonard J; GeneDx, Inc, Gaithersburg, MD, USA.
  • Lin K; Individualized Medical Genetic Center, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Medne L; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Santani A; Individualized Medical Genetic Center, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Skraban C; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Yang S; Individualized Medical Genetic Center, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Ahrens-Nicklas RC; GeneDx, Inc, Gaithersburg, MD, USA.
Genet Med ; 22(2): 423-426, 2020 02.
Article in En | MEDLINE | ID: mdl-31527676
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Exome Sequencing / Heart Failure Type of study: Prognostic_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2020 Type: Article Affiliation country: United States
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Testing / Exome Sequencing / Heart Failure Type of study: Prognostic_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2020 Type: Article Affiliation country: United States