Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and GRHL3[original query] |
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Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population. PloS one 2016 11 (7): e0159940. He Miao, Bian Zhu |
Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort. Gene 2016 Apr . Wang Yirui, Sun Yimin, Huang Yongqing, Pan Yongchu, Jia Zhonglin, Ma Lijuan, Ma Lan, Lan Feifei, Zhou Yuxi, Shi Jiayu, Yang Xiong, Zhang Lei, Jiang Hongbing, Jiang Min, Yin Aihua, Cheng Jing, Wang Lin, Yang Yinxue, Shi Bi |
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate. American journal of human genetics 2016 Mar . Mangold Elisabeth, Böhmer Anne C, Ishorst Nina, Hoebel Ann-Kathrin, Gültepe Pinar, Schuenke Hannah, Klamt Johanna, Hofmann Andrea, Gölz Lina, Raff Ruth, Tessmann Peter, Nowak Stefanie, Reutter Heiko, Hemprich Alexander, Kreusch Thomas, Kramer Franz-Josef, Braumann Bert, Reich Rudolf, Schmidt Gül, Jäger Andreas, Reiter Rudolf, Brosch Sibylle, Stavusis Janis, Ishida Miho, Seselgyte Rimante, Moore Gudrun E, Nöthen Markus M, Borck Guntram, Aldhorae Khalid A, Lace Baiba, Stanier Philip, Knapp Michael, Ludwig Kerstin |
Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate. Journal of dental research 2017 Sep 22034517729819. Eshete M A, Liu H, Li M, Adeyemo W L, Gowans L J J, Mossey P A, Busch T, Deressa W, Donkor P, Olaitan P B, Aregbesola B S, Braimah R O, Oseni G O, Oginni F, Audu R, Onwuamah C, James O, Augustine-Akpan E, Rahman L A, Ogunlewe M O, Arthur F K N, Bello S A, Agbenorku P, Twumasi P, Abate F, Hailu T, Demissie Y, Hailu A, Plange-Rhule G, Obiri-Yeboah S, Dunnwald M M, Gravem P E, Marazita M L, Adeyemo A A, Murray J C, Cornell R A, Butali |
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- Page last updated:Apr 22, 2024
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