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Copy number alterations involving 59 ACMG-recommended secondary findings genes.
Yatsenko, Svetlana A; Aarabi, Mahmoud; Hu, Jie; Surti, Urvashi; Ortiz, Damara; Madan-Khetarpal, Suneeta; Saller, Devereux N; Bellissimo, Daniel; Rajkovic, Aleksandar.
Affiliation
  • Yatsenko SA; Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Aarabi M; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Hu J; Magee-Womens Research Institute, Pittsburgh, Pennsylvania, USA.
  • Surti U; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Ortiz D; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Madan-Khetarpal S; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Saller DN; Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Bellissimo D; Department of Medical Genetics, Childrens Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
  • Rajkovic A; Department of Medical Genetics, Childrens Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
Clin Genet ; 98(6): 577-588, 2020 12.
Article in En | MEDLINE | ID: mdl-33009833
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cytogenetic Analysis / Genomics / DNA Copy Number Variations / Exome Sequencing Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Clin Genet Year: 2020 Document type: Article Affiliation country: Estados Unidos
Fulltext
Add to My VHL
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cytogenetic Analysis / Genomics / DNA Copy Number Variations / Exome Sequencing Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Clin Genet Year: 2020 Document type: Article Affiliation country: Estados Unidos