Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate

American Journal of Human Genetics

Volumn 98, Issue 4, 2016, Pages 755-762

  Mangold, Elisabeth ^a   Böhmer, Anne C ^a   Ishorst, Nina ^a   Hoebel, Ann Kathrin ^a   Gültepe, Pinar ^a   Schuenke, Hannah ^a   Klamt, Johanna ^a   Hofmann, Andrea ^a   Gölz, Lina ^a   Raff, Ruth ^a   Tessmann, Peter ^a   Nowak, Stefanie ^a   Reutter, Heiko ^a   Hemprich, Alexander ^b   Kreusch, Thomas ^c   Kramer, Franz Josef ^d   Braumann, Bert ^e   Reich, Rudolf ^a   Schmidt, Gül ^f   Jäger, Andreas ^a   Reiter, Rudolf ^g   Brosch, Sibylle ^g   Stavusis, Janis ^h   Ishida, Miho ⁱ   Seselgyte, Rimante ⁱ   Moore, Gudrun E ⁱ   Nöthen, Markus M ^a   Borck, Guntram ^g   Aldhorae, Khalid A ^j   Lace, Baiba ^h   Stanier, Philip ⁱ   Knapp, Michael ^a   Ludwig, Kerstin U ^a   more..

^a UNIVERSITY OF BONN   (Germany)

^b UNIVERSITY HOSPITAL LEIPZIG   (Germany)

^c Asklepios Klinik Nord Heidberg   (Germany)

^d UNIVERSITY OF GÖTTINGEN   (Germany)

^e UNIVERSITY OF COLOGNE   (Germany)

^f HUMBOLDT UNIVERSITY   (Germany)

^g UNIVERSITY OF ULM   (Germany)

^h LATVIAN BIOMEDICAL RESEARCH AND STUDY CENTRE   (Latvia)

ⁱ UNIVERSITY COLLEGE LONDON   (United Kingdom)

^j THAMAR UNIVERSITY   (Yemen)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ALLELISM; ARTICLE; CLEFT PALATE; CONTROLLED STUDY; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GRAINY HEAD LIKE 3 GENE; HUMAN; LATVIA; MARKER GENE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; UNITED KINGDOM; VAN DER WOUDE SYNDROME; YEMEN; ABNORMALITIES; ABNORMALITIES, MULTIPLE; ALLELE; ANCESTRY GROUP; CASE CONTROL STUDY; CLEFT LIP; CYSTS; GENETIC PREDISPOSITION; GENETICS; LIP; MUTATION; OPEN READING FRAME; SINGLE NUCLEOTIDE POLYMORPHISM;

DNA BINDING PROTEIN; GRHL3 PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

ABNORMALITIES, MULTIPLE; ALLELES; CASE-CONTROL STUDIES; CLEFT LIP; CLEFT PALATE; CONTINENTAL POPULATION GROUPS; CYSTS; DNA-BINDING PROTEINS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LIP; MUTATION; OPEN READING FRAMES; POLYMORPHISM, SINGLE NUCLEOTIDE; TRANSCRIPTION FACTORS;

EID: 84964894086     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2016.02.013     Document Type: Article

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