Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Taurodontism[original query] |
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Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies. Indian journal of dentistry 2014 Oct 5 (4): 172-82. Ceyhan Derya, Kirzioglu Zuhal, Calapoglu Nilufer Sah |
GREM2 nucleotide variants and the risk of tooth agenesis. Oral diseases 2017 Oct . Mostowska A, Biedziak B, Zadurska M, Bogdanowicz A, Olszewska A, Cie?li?ska K, Firlej E, Jagodzi?ski P |
WNT10B mutations associated with isolated dental anomalies. Clinical genetics 2018 1 93 (5): 992-999. Kantaputra P N, Hutsadaloi A, Kaewgahya M, Intachai W, German R, Koparal M, Leethanakul C, Tolun A, Ketudat Cairns J |
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- Page last updated:Apr 29, 2024
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