Whole Exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

Genetics

Volumn 197, Issue 3, 2014, Pages 1039-1044

  Bureau, Alexandre ^a   Parker, Margaret M ^b   Ruczinski, Ingo ^c   Taub, Margaret A ^c   Marazita, Mary L ^d   Murray, Jeffrey C ^e   Mangold, Elisabeth ^f   Noethen, Markus M ^f   Ludwig, Kirsten U ^f   Hetmanski, Jacqueline B ^b   Bailey Wilson, Joan E ^g   Cropp, Cheryl D ^g   Li, Qing ^g   Szymczak, Silke ^g   Albacha Hejazi, Hasan ^h   Alqosayer, Khalid ⁱ   Leigh Field, L ^j   Wu Chou, Yah Huei ^k   Doheny, Kimberly F ^l   Ling, Hua ^l   Scott, Alan F ^l   Beaty, Terri H ^b   more..

^a CENTRE DE RECHERCHE DE L INSTITUT UNIVERSITAIRE EN SANTÉ MENTALE DE QUÉBEC   (Canada)

^b JOHNS HOPKINS UNIVERSITY   (United States)

^c JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

^d UNIVERSITY OF PITTSBURGH   (United States)

^e UNIVERSITY OF IOWA   (United States)

^f UNIVERSITY OF BONN   (Germany)

^g NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^h Hejazi Clinic   (Saudi Arabia)

ⁱ Prime Health Clinic Jeddah   (Saudi Arabia)

^j UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^k CHANG GUNG MEMORIAL HOSPITAL   (Taiwan)

^l JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CLEFT LIP; CLEFT PALATE; DNA SEQUENCE; EXOME; FEMALE; GENE; GENE IDENTIFICATION; GENE SEQUENCE; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; ORAL DRUG ADMINISTRATION; PEDIGREE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; WHOLE EXOME SEQUENCING; ETHNIC GROUP; FAMILY; GENETIC ASSOCIATION; GENETICS; MUTATION; PROCEDURES; REPRODUCIBILITY;

CADHERIN; CDH1 PROTEIN, HUMAN;

CADHERINS; CLEFT PALATE; ETHNIC GROUPS; EXOME; FAMILY; FEMALE; GENETIC ASSOCIATION STUDIES; HUMANS; MALE; MUTATION; PEDIGREE; REPRODUCIBILITY OF RESULTS; SEQUENCE ANALYSIS, DNA;

EID: 84904246196     PISSN: 00166731     EISSN: 19432631     Source Type: Journal    
DOI: 10.1534/genetics.114.165225     Document Type: Article

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