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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

235 related items for PubMed ID: 24700731

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  • 2. Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia.
    Yu M, Liu Y, Liu H, Wong SW, He H, Zhang X, Wang Y, Han D, Feng H.
    Am J Med Genet A; 2019 Jan; 179(1):57-64. PubMed ID: 30569517
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  • 8. Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia.
    Liu Y, Sun J, Zhang C, Wu Y, Ma S, Li X, Wu X, Gao Q.
    BMC Oral Health; 2024 Jan 27; 24(1):136. PubMed ID: 38280992
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  • 12. WNT10A variants are associated with non-syndromic tooth agenesis in the general population.
    Song S, Zhao R, He H, Zhang J, Feng H, Lin L.
    Hum Genet; 2014 Jan 27; 133(1):117-24. PubMed ID: 24043634
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  • 15. Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.
    Tardieu C, Jung S, Niederreither K, Prasad M, Hadj-Rabia S, Philip N, Mallet A, Consolino E, Sfeir E, Noueiri B, Chassaing N, Dollfus H, Manière MC, Bloch-Zupan A, Clauss F.
    Clin Genet; 2017 Nov 27; 92(5):477-486. PubMed ID: 28105635
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  • 16. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing.
    Zhao K, Lian M, Zou D, Huang W, Zhou W, Shen Y, Wang F, Wu Y.
    Oral Dis; 2019 Mar 27; 25(2):523-534. PubMed ID: 30417976
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  • 19. WNT10B mutations associated with isolated dental anomalies.
    Kantaputra PN, Hutsadaloi A, Kaewgahya M, Intachai W, German R, Koparal M, Leethanakul C, Tolun A, Ketudat Cairns JR.
    Clin Genet; 2018 May 27; 93(5):992-999. PubMed ID: 29364501
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