HuGE Literature Finder
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| Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing Study. Frontiers in genetics 2022 3 13 828534. Lace Baiba, Pajusalu Sander, Livcane Diana, Grinfelde Ieva, Akota Ilze, Mauli?a Ieva, Bark?ne Biruta, Stavusis Janis, Inashkina In |
| Two promoter polymorphisms in TBX22 are associated with the risk of NSCLP in Indian women. Clinical dysmorphology 2015 Oct 24 (4): 140-3. Gurramkonda Venkatesh B, Hussain Syed A, Murthy Jyotsna, Lakkakula Bhaskar V K |
| Non-syndromic cleft palate: analysis of TBX22 exon 5 gene mutation. Archives of medical science : AMS 2012 Jul 8 (3): 406-10. Jiang Run-Song, Zhao Xiong, Liu R |
| A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia. Journal of medical genetics 2009 Aug 46 (8): 555-61. Pauws E, Moore G E, Stanier |
| TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population. Clinical genetics 2007 Nov 72 (5): 478-83. Suphapeetiporn K, Tongkobpetch S, Siriwan P, Shotelersuk |
| PAX9 and TGFB3 are linked to susceptibility to nonsyndromic cleft lip with or without cleft palate in the Japanese: population-based and family-based candidate gene analyses. Journal of human genetics 2006 51 (1): 38-46. Ichikawa Eisaburo, Watanabe Akira, Nakano Yoko, Akita Sadanori, Hirano Akiyoshi, Kinoshita Akira, Kondo Shinji, Kishino Tatsuya, Uchiyama Takeshi, Niikawa Norio, Yoshiura Koh-ichi |
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