Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.

Content Provider	Europe PMC
Author	Ishorst, Nina Henschel, Leonie Thieme, Frederic Drichel, Dmitriy Sivalingam, Sugirthan Mehrem, Sarah L. Fechtner, Ariane C. Fazaal, Julia Welzenbach, Julia Heimbach, André Maj, Carlo Borisov, Oleg Hausen, Jonas Raff, Ruth Hoischen, Alexander Dixon, Michael Rada‐Iglesias, Alvaro Bartusel, Michaela Rojas‐Martinez, Augusto Aldhorae, Khalid Braumann, Bert Kruse, Teresa Kirschneck, Christian Spanier, Gerrit Reutter, Heiko Nowak, Stefanie Gölz, Lina Knapp, Michael Buness, Andreas Krawitz, Peter Nöthen, Markus M. Nothnagel, Michael Becker, Tim Ludwig, Kerstin U. Mangold, Elisabeth
Page Count	16
Journal	Molecular Genetics & Genomic Medicine
Volume Number	11
PubMed Central reference number	PMC10009911
Issue Number	3
PubMed reference number	36468602
e-ISSN	23249269
DOI	10.1002/mgg3.2109
Language	English
Publisher	John Wiley and Sons Inc.
Publisher Date	2022-12-05
Publisher Place	Hoboken
Access Restriction	Open
Rights License	This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. © 2022 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC.
Subject Keyword	candidate genes de novo variants exome sequencing nonsyndromic cleft lip with/without cleft palate polygenic risk single‐molecule molecular inversion probes
Content Type	Text
Resource Type	Article
Subject	Genetics Molecular Biology Genetics (clinical)