Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: TBX22[original query] |
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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 |
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 |
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 |
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 |
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 |
Genetic landscape of autism spectrum disorder in Vietnamese children. Scientific reports 2020 3 10 (1): 5034. Tran Kien Trung, Le Vinh Sy, Bui Hoa Thi Phuong, Do Duong Huy, Ly Ha Thi Thanh, Nguyen Hieu Thi, Dao Lan Thi Mai, Nguyen Thanh Hong, Vu Duc Minh, Ha Lien Thi, Le Huong Thi Thanh, Mukhopadhyay Arijit, Nguyen Liem Tha |
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 |
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- Page last updated:Apr 22, 2024
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