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Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data.
Guo, Michael H; Plummer, Lacey; Chan, Yee-Ming; Hirschhorn, Joel N; Lippincott, Margaret F.
Afiliação
  • Guo MH; Division of Endocrinology, Department of Pediatrics, Boston Children's Hospital, Boston, MA 02115, USA; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA 02142, USA; Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Plummer L; Division of Endocrinology, Reproductive Endocrine Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Chan YM; Division of Endocrinology, Department of Pediatrics, Boston Children's Hospital, Boston, MA 02115, USA.
  • Hirschhorn JN; Division of Endocrinology, Department of Pediatrics, Boston Children's Hospital, Boston, MA 02115, USA; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA 02142, USA; Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Lippincott MF; Division of Endocrinology, Reproductive Endocrine Unit, Massachusetts General Hospital, Boston, MA 02114, USA. Electronic address: mlippincott@mgh.harvard.edu.
Am J Hum Genet ; 103(4): 522-534, 2018 10 04.
Article em En | MEDLINE | ID: mdl-30269813
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Exoma Idioma: En Ano de publicação: 2018 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 Assunto principal: Polimorfismo de Nucleotídeo Único / Exoma Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos