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Volumn 98, Issue 4, 2016, Pages 744-754

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3

(58)  Leslie, Elizabeth J a   Liu, Huan b,c   Carlson, Jenna C a,d   Shaffer, John R a,d   Feingold, Eleanor a,d   Wehby, George e   Laurie, Cecelia A f   Jain, Deepti f   Laurie, Cathy C f   Doheny, Kimberly F g   McHenry, Toby a   Resick, Judith a   Sanchez, Carla a   Jacobs, Jennifer a   Emanuele, Beth a   Vieira, Alexandre R a,d   Neiswanger, Katherine a   Standley, Jennifer b   Czeizel, Andrew E h   Deleyiannis, Frederic i   more..


Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLEFT PALATE; EMBRYO; GENE FUNCTION; GENE SEQUENCE; GENETIC RISK; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GRHL3 GENE; HUMAN; MARKER GENE; MISSENSE MUTATION; NONHUMAN; NONSYNDROMIC CLEFT PALATE; PRIORITY JOURNAL; RISK FACTOR; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; TRANSACTIVATION; ZEBRA FISH; ANIMAL; CASE CONTROL STUDY; DISEASE MODEL; EMBRYOLOGY; ETHNIC GROUP; GENE LOCUS; GENETICS; GENOTYPING TECHNIQUE;

EID: 84964895172     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2016.02.014     Document Type: Article
Times cited : (124)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.