IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families

Clinical Genetics

Volumn 90, Issue 1, 2016, Pages 28-34

  Leslie, E J ^a   Koboldt, D C ^b   Kang, C J ^b   Ma, L ^c   Hecht, J T ^d   Wehby, G L ^e   Christensen, K ^f   Czeizel, A E ^g   Deleyiannis, F W B ^h   Fulton, R S ^b   Wilson, R K ^b   Beaty, T H ⁱ   Schutte, B C ^j   Murray, J C ^k   Marazita, M L ^a  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c PEKING UNIVERSITY SCHOOL AND HOSPITAL OF STOMATOLOGY   (China)

^d UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^e UNIVERSITY OF IOWA   (United States)

^f UNIVERSITY OF SOUTHERN DENMARK   (Denmark)

^g FOUNDATION FOR THE COMMUNITY CONTROL OF HEREDITARY DISEASES   (Hungary)

^h UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

ⁱ JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

^j Michigan State University ^*  (United States)

^k UNIVERSITY OF IOWA   (United States)

more..

Author keywords

interferon regulatory factor 6; mutation screening; non syndromic oral clefts; syndromic cleft

Indexed keywords

INTERFERON REGULATORY FACTOR 6;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CLEFT LIP; CLEFT PALATE; CONTROLLED STUDY; GENETIC POLYMORPHISM; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; PEDIGREE; PRIORITY JOURNAL; VAN DER WOUDE SYNDROME;

EID: 84973610971     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/cge.12675     Document Type: Article

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