TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population

Author:

Suphapeetiporn K,Tongkobpetch S,Siriwan P,Shotelersuk V

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. Classification and birth prevalence of orofacial clefts;Tolarova;Am J Med Genet,1998

2. The many faces and factors of orofacial clefts;Schutte;Hum Mol Genet,1999

3. Genetics of cleft lip and palate;Bender;J Pediatr Nurs,2000

4. A novel mutation, 1234del(C), of the IRF6 in a Thai family with Van der Woude syndrome;Shotelersuk;Int J Mol Med,2003

5. De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndrome;Shotelersuk;Clin Exp Dermatol,2005

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1. Two Novel Missense Tbx22 Mutations Frequently Cause Non-Syndromic Cleft Palate in Pakistani Population;Pakistan Journal of Zoology;2022

2. Genetic Factors Responsible for Cleft Lip and Palate;Surgical Atlas of Cleft Palate and Palatal Fistulae;2022

3. Genetic Factors Responsible for Cleft Lip and Palate;Surgical Atlas of Cleft Palate and Palatal Fistulae;2022

4. Genetic Factors Responsible for Cleft Lip and Palate;Surgical Atlas of Cleft Palate and Palatal Fistulae;2022

5. Essential role of Msx1 in regulating anterior-posterior patterning of the secondary palate in mice;Journal of Genetics and Genomics;2021-07

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