ZFHX4 truncating variant and orofacial clefting
- PMID: 37434517
- DOI: 10.1002/ajmg.a.63353
ZFHX4 truncating variant and orofacial clefting
Comment on
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Concurrent de novo ZFHX4 variant and 16q24.1 deletion in a patient with orofacial clefting; a potential role of ZFHX4 and USP10.Am J Med Genet A. 2023 Apr;191(4):1083-1088. doi: 10.1002/ajmg.a.63101. Epub 2023 Jan 3. Am J Med Genet A. 2023. PMID: 36595458
References
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- Créton, M., Wagener, F., Massink, M., Fennis, W., Bloemen, M., Schols, J., Aarts, M., van der Molen, A. M., van Haaften, G., & van den Boogaard, M. J. (2023). Concurrent de novo ZFHX4 variant and 16q24.1 deletion in a patient with orofacial clefting; a potential role of ZFHX4 and USP10. American Journal of Medical Genetics Part A, 191(4), 1083-1088. https://doi.org/10.1002/ajmg.a.63101
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- Richards, S., Aziz, N., Bale, S., Bick, D., Das, S., Gastier-Foster, J., Grody, W. W., Hegde, M., Lyon, E., Spector, E., Voelkerding, K., Rehm, H. L., & ACMG Laboratory Quality Assurance Committee. (2015). Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 17(5), 405-424. https://doi.org/10.1038/gim.2015.30
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