Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.
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| Title: | Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts. |
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| Authors: | Bureau A; Centre de Recherche de l'Institut Universitaire en Santé Mentale de Québec and Département de Médecine Sociale et Préventive, Université Laval, Québec, QC G1V 0A6, Canada., Parker MM; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205., Ruczinski I; Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205., Taub MA; Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205., Marazita ML; Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15219., Murray JC; Department of Pediatrics, School of Medicine, University of Iowa, Iowa City, Iowa 52242., Mangold E; Institute of Human Genetics, University of Bonn, Bonn, Germany D-53111., Noethen MM; Institute of Human Genetics, University of Bonn, Bonn, Germany D-53111., Ludwig KU; Institute of Human Genetics, University of Bonn, Bonn, Germany D-53111., Hetmanski JB; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205., Bailey-Wilson JE; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121., Cropp CD; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121., Li Q; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121., Szymczak S; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121., Albacha-Hejazi H; Hejazi Clinic, Clinic, Riyadh, Saudia Arabia 11461., Alqosayer K; Prime Health Clinic, Jeddah, Saudi Arabia 21511., Field LL; Department of Human Genetics, University of British Columbia, Vancouver, Canada V6T1Z3., Wu-Chou YH; Laboratory of Human Molecular Genetics, Chang Gung Memorial Hospital, Taipei, Taiwan 333., Doheny KF; Center for Inherited Disease Research, Johns Hopkins School of Medicine, Baltimore Maryland 21224., Ling H; Center for Inherited Disease Research, Johns Hopkins School of Medicine, Baltimore Maryland 21224., Scott AF; Institute of Genetic Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland 21224., Beaty TH; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205 tbeaty1@jhu.edu. |
| Source: | Genetics [Genetics] 2014 Jul; Vol. 197 (3), pp. 1039-44. Date of Electronic Publication: 2014 May 02. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Oxford University Press Country of Publication: United States NLM ID: 0374636 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1943-2631 (Electronic) Linking ISSN: 00166731 NLM ISO Abbreviation: Genetics Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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