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

Erstveröffentlichung
2016
Authors
Mangold, Elisabeth
Boehmer, Anne C.
Ishorst, Nina
Hoebel, Ann-Kathrin
Gueltepe, Pinar
et al.
Wissenschaftlicher Artikel


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
Institutions
UKU. Klinik für Hals-, Nasen-, Ohrenheilkunde, Kopf- und Halschirurgie
UKU. Institut für Humangenetik
Subject headings
[DDC subject group]: DDC 610 / Medicine & health

Metadata
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