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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 6, 2024. (Total: 234148Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Cleft Palate and FGFR2[original query]
Testing reported associations of genetic risk factors for oral clefts in a large Irish study population.
Birth defects research. Part A, Clinical and molecular teratology 2010 Feb 88 (2): 84-93.
Carter Tonia C, Molloy Anne M, Pangilinan Faith, Troendle James F, Kirke Peadar N, Conley Mary R, Orr David J A, Earley Michael, McKiernan Eamon, Lynn Ena C, Doyle Anne, Scott John M, Brody Lawrence C, Mills James
The FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2013 Jan 50 (1): 96-103.
Wang Hong, Zhang Tianxiao, Wu Tao, Hetmanski Jacqueline B, Ruczinski Ingo, Schwender Holger, Liang Kung Yee, Murray Tanda, Fallin M Daniele, Redett Richard J, Raymond Gerald V, Jin Sheng-Chih, Chou Yah-Huei Wu, Chen Philip Kuo-Ting, Yeow Vincent, Chong Samuel S, Cheah Felicia S H, Jee Sun Ha, Jabs Ethylin W, Scott Alan F, Beaty Terri
Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.
American journal of human genetics 2015 Mar 96 (3): 397-411.
Leslie Elizabeth J, Taub Margaret A, Liu Huan, Steinberg Karyn Meltz, Koboldt Daniel C, Zhang Qunyuan, Carlson Jenna C, Hetmanski Jacqueline B, Wang Hang, Larson David E, Fulton Robert S, Kousa Youssef A, Fakhouri Walid D, Naji Ali, Ruczinski Ingo, Begum Ferdouse, Parker Margaret M, Busch Tamara, Standley Jennifer, Rigdon Jennifer, Hecht Jacqueline T, Scott Alan F, Wehby George L, Christensen Kaare, Czeizel Andrew E, Deleyiannis Frederic W-B, Schutte Brian C, Wilson Richard K, Cornell Robert A, Lidral Andrew C, Weinstock George M, Beaty Terri H, Marazita Mary L, Murray Jeffrey
Exploring the interaction between FGF Genes and T-box genes among chinese nonsyndromic cleft lip with or without cleft palate case-parent trios.
Environmental and molecular mutagenesis 2019 Mar .
Li Wenyong, Wang Mengying, Zhou Ren, Wang Siyue, Zheng Hongchen, Liu Dongjing, Zhou Zhibo, Zhu Hongping, Wu Tao, Beaty Terri
Hearing, Speech, Language, and Communicative Participation in Patients With Apert Syndrome: Analysis of Correlation With Fibroblast Growth Factor Receptor 2 Mutation.
The Journal of craniofacial surgery 2021 Jul .
Kilcoyne Sarah, Luscombe Carrie, Scully Paula, Overton Sarah, Brockbank Sally, Swan Marc C, Johnson David, Wall Steven, Wilkie Andrew O
Genetic variations at 10q26 regions near FGFR2 gene and its association with non-syndromic cleft lip with or without cleft palate.
International journal of pediatric otorhinolaryngology 2021 3 143 110648.
Raju Ginila T, L V K S Bhaskar, Gurramkonda Venkatesh Babu, Hussain Syed Altaf, Paul Solomon F
Integrating transcriptomics and genomics to identify fibroblast growth factor/receptor candidate genes for non-syndromic orofacial cleft in Chinese.
Archives of oral biology 2023 6 153 105750.
Bin Ge, Yansong Lin, Bing Shi, Zhonglin J
Dental Anomalies and Genetic Polymorphisms as Predictors of Maxillofacial Growth in Individuals Born with Cleft Lip and Palate.
Journal of dental research 2023 6 220345231169915.
R H W Lacerda, A R Viei
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