Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations
Author:
Funder
German Research Foundation
Publisher
Elsevier BV
Subject
Genetics (clinical),Molecular Medicine
Reference54 articles.
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3. Risk of oral clefts in twins;Grosen;Epidemiology,2011
4. Integrative approaches generate insights into the architecture of non-syndromic cleft lip ± cleft palate;Welzenbach;HGG Adv.,2021
5. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes;Basha;J. Med. Genet.,2018
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1. Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?;American Journal of Medical Genetics Part A;2023-06-23
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