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Deletion of conserved non-coding sequences downstream from NKX2-1: A novel disease-causing mechanism for benign hereditary chorea.
Liao, Jun; Coffman, Keith A; Locker, Joseph; Padiath, Quasar S; Nmezi, Bruce; Filipink, Robyn A; Hu, Jie; Sathanoori, Malini; Madan-Khetarpal, Suneeta; McGuire, Marianne; Schreiber, Allison; Moran, Rocio; Friedman, Neil; Hoffner, Lori; Rajkovic, Aleksandar; Yatsenko, Svetlana A; Surti, Urvashi.
Afiliação
  • Liao J; Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.
  • Coffman KA; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
  • Locker J; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Padiath QS; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Nmezi B; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
  • Filipink RA; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
  • Hu J; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Sathanoori M; Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.
  • Madan-Khetarpal S; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
  • McGuire M; Pittsburgh Cytogenetics Laboratory, Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA.
  • Schreiber A; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Moran R; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
  • Friedman N; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Hoffner L; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Rajkovic A; Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Yatsenko SA; Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Surti U; Center for Pediatric Neurology, Cleveland Clinic, Cleveland, OH, USA.
Mol Genet Genomic Med ; 9(4): e1647, 2021 04.
Article em En | MEDLINE | ID: mdl-33666368
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sequências Reguladoras de Ácido Nucleico / Coreia / Fator Nuclear 1 de Tireoide Tipo de estudo: Prognostic_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sequências Reguladoras de Ácido Nucleico / Coreia / Fator Nuclear 1 de Tireoide Tipo de estudo: Prognostic_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos