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Congenital hypothyroidism, spiky hair, and cleft palate
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A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis
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A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate
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Association of candidate genes with nonsyndromic clefts in Honduran and Colombian populations
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Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results
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Marazita, M. L., Lidral, A. C., Murray, J. C., Field, L. L., Maher, B. S., Goldstein McHenry, T., Cooper, M. E., Govil, M., Daack-Hirsch, S., Riley, B., Jugessur, A., Felix, T., Morene, L., Mansilla, M. A., Vieira, A. R., Doheny, K., Pugh, E., Valencia-Ramirez, C. & Arcos-Burgos, M. (2009). Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results. Human Heredity 68, 151-170.
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Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate
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Nikopensius, T., Kempa, I., Ambrozaityte, L., Jagomagi, T., Saag, M., Matuleviciene, A., Utkus, A., Krjutskov, K., Tammekivi, V., Piekuse, L., Akota, I., Barkane, B., Krumina, A., Klovins, J., Lace, B., Kucinskas, V. & Metspalu, A. (2011). Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate. Birth Defects Research Part A, Clinical Molecular Teratology 91, 218-225.
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9
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PDGFRa mutations in humans with isolated cleft palate
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Rattanasopha, S., Tongkobpetch, S., Srichomthong, C., Siriwan, P., Suphapeetiporn, K. & Shotelersuk, V. (2012). PDGFRa mutations in humans with isolated cleft palate. European Journal of Human Genetics 20, 1058-1062.
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Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip
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Shotelersuk, V., Ittiwut, C., Siriwan, P. & Angspatt, A. (2003). Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip. Journal of Medical Genetics 40, e64.
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TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population
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Suphapeetiporn, K., Tongkobpetch, S., Siriwan, P. & Shotelersuk, V. (2007). TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population. Clinical Genetics 72, 478-483.
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12
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MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population
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Tongkobpetch, S., Siriwan, P. & Shotelersuk, V. (2006). MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population. Journal of Human Genetics 51, 671-676.
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Tongkobpetch, S.1
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13
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Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate
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Tongkobpetch, S., Suphapeetiporn, K., Siriwan, P. & Shotelersuk, V. (2008). Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate. International Journal of Oral Maxillofacial Surgery 37, 550-553.
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14
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58149149907
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Altered binding of MYF-5 to FOXE1 promoter in non-syndromic and CHARGEassociated cleft palate
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Venza, M., Visalli, M., Venza, I., Torino, C., Tripodo, B., Melita, R. & Teti, D. (2009). Altered binding of MYF-5 to FOXE1 promoter in non-syndromic and CHARGEassociated cleft palate. Journal of Oral Pathology & Medicine 38, 18-23.
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15
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Unraveling human cleft lip and palate research
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Vieira, A. R. (2008). Unraveling human cleft lip and palate research. Journal of Dental Research 87, 119-125.
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Vieira, A.R.1
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16
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Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome
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Yeetong, P., Mahatumarat, C., Siriwan, P., Rojvachiranonda, N., Suphapeetiporn, K. & Shotelersuk, V. (2009). Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome. American Journal of Medical Genetics A 149A, 2489-2492.
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Yeetong, P.1
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