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Rare genetic variants in SEC24D modify orofacial cleft phenotypes.
Curtis, Sarah W; Carlson, Jenna C; Beaty, Terri H; Murray, Jeffrey C; Weinberg, Seth M; Marazita, Mary L; Cotney, Justin L; Cutler, David J; Epstein, Michael P; Leslie, Elizabeth J.
Affiliation
  • Curtis SW; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.
  • Carlson JC; Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, 15621, USA.
  • Beaty TH; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
  • Murray JC; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 21205,USA.
  • Weinberg SM; Department of Pediatrics, University of Iowa, Iowa City, IA, 52242, USA.
  • Marazita ML; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
  • Cotney JL; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
  • Cutler DJ; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
  • Epstein MP; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
  • Leslie EJ; Department of Genetics and Genome Sciences, University of Connecticut, CT, 06030, USA.
medRxiv ; 2023 Mar 27.
Article in En | MEDLINE | ID: mdl-37034635

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: MedRxiv Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: MedRxiv Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos