Rare genetic variants in SEC24D modify orofacial cleft phenotypes.
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| Title: | Rare genetic variants in SEC24D modify orofacial cleft phenotypes. |
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| Authors: | 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.; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA., Beaty TH; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 21205,USA., Murray JC; Department of Pediatrics, University of Iowa, Iowa City, IA, 52242, USA., Weinberg SM; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA, 15261, USA., Marazita ML; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA, 15261, USA., Cotney JL; Department of Genetics and Genome Sciences, University of Connecticut, CT, 06030, USA., Cutler DJ; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA., Epstein MP; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA., Leslie EJ; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA. |
| Source: | MedRxiv : the preprint server for health sciences [medRxiv] 2023 Mar 27. Date of Electronic Publication: 2023 Mar 27. |
| Publication Type: | Preprint; Journal Article |
| Journal Info: | Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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