Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate-Reference-Cited by-同舟云学术

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

Published:2016-04 Issue:4 Volume:98 Page:755-762
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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