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

Mangold, Elisabeth; Boehmer, Anne C.; Ishorst, Nina; Hoebel, Ann-Kathrin; Gueltepe, Pinar; Schuenke, Hannah; Klamt, Johanna; Hofmann, Andrea; Goelz, Lina; Raff, Ruth; Tessmann, Peter; Nowak, Stefanie; Reutter, Heiko; Hemprich, Alexander; Kreusch, Thomas; Kramer, Franz-Josef; Braumann, Bert; Reich, Rudolf; Schmidt, Guel; Jaeger, Andreas; Reiter, Rudolf; Brosch, Sibylle; Stavusis, Janis; Ishida, Miho; Seselgyte, Rimante; Moore, Gudrun E.; Noethen, Markus M.; Borck, Guntram; Aldhorae, Khalid A.; Lace, Baiba; Stanier, Philip; Knapp, Michael; Ludwig, Kerstin U.

Erstveröffentlichung

2016

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Wissenschaftlicher Artikel

Authors

Mangold, Elisabeth

Boehmer, Anne C.

Ishorst, Nina

Hoebel, Ann-Kathrin

Gueltepe, Pinar

et al.

Institutions

UKU. Klinik für Hals-, Nasen-, Ohrenheilkunde, Kopf- und Halschirurgie
UKU. Institut für Humangenetik

Published in

American Journal of Human Genetics ; 98 (2016), 4. - S. 755-762. - ISSN 0002-9297. - eISSN 1537-6605

Link to publication

https://dx.doi.org/10.1016/j.ajhg.2016.02.013

Funding information

Deutsche Forschungsgemeinschaft (DFG) [FOR 423, MA 2546/3-1, MA 2546/5-1, LU 1944/2-1, KR 1912/7-1, NO 246/6-1, WI 1555/5-1]
BONFOR program of the Medical Faculty Bonn [0-149.0097]
National Institute for Health Research Biomedical Research Centre at Great Ormond Street Hospital for Children NHS Foundation Trust and University College London

Dewey Decimal Group

DDC 610 / Medicine & health

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