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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 18 (of 18 Records)

Query Trace: Syndrome and IRF6[original query]
Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations.
Genetics in medicine : official journal of the American College of Medical Genetics 2007 Apr 9 (4): 219-27.
Park Ji Wan, McIntosh Iain, Hetmanski Jacqueline B, Jabs Ethylin Wang, Vander Kolk Craig A, Wu-Chou Yah-Huei, Chen Philip K, Chong Samuel S, Yeow Vincent, Jee Sun Ha, Park Beyoung Yun, Fallin M Daniele, Ingersoll Roxann, Scott Alan F, Beaty Terri
Evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and isolate tooth agenesis, in a Turkish population.
Archives of oral biology 2008 Aug 53 (8): 780-4.
Vieira Alexandre R, Seymen Figen, Patir Asli, Menezes Rena
Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway.
Genetic epidemiology 2008 Jul 32 (5): 413-24.
Jugessur Astanand, Rahimov Fedik, Lie Rolv T, Wilcox Allen J, Gjessing Håkon K, Nilsen Roy M, Nguyen Truc Trung, Murray Jeffrey
Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.
European journal of orthodontics 2008 Apr 30 (2): 169-75.
Pegelow M, Peyrard-Janvid M, Zucchelli M, Fransson I, Larson O, Kere J, Larsson C, Karsten
The association between interferon regulatory factor 6 (IRF6) and nonsyndromic cleft lip with or without cleft palate in a Honduran population.
The Laryngoscope 2009 Jun .
Diercks GR, Karnezis TT, Kent DT, Flores C, Su GH, Lee JH, Haddad J
Mutation screening of IRF6 among families with non-syndromic oral clefts and identification of two novel variants: review of the literature.
European journal of medical genetics 2012 Jun 55 (6-7): 389-93.
Salahshourifar Iman, Wan Sulaiman Wan Azman, Halim Ahmad Sukari, Zilfalil Bin Al
Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes.
American journal of medical genetics. Part A 2013 Oct 161A (10): 2535-44.
Leslie Elizabeth J, Mancuso Jennifer L, Schutte Brian C, Cooper Margaret E, Durda Kate M, L'heureux Jamie, Zucchero Theresa M, Marazita Mary L, Murray Jeffrey
Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2013 Feb .
Pegelow M, Koillinen H, Magnusson M, Fransson I, Unneberg P, Kere J, Karsten A, Peyrard-Janvid M
Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial Clefting.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2015 Sep 52 (5): e161-7.
Charzewska Agnieszka, Obersztyn Ewa, Hoffman-Zacharska Dorota, Lenart Jacek, Pozna?ski Jaros?aw, Bal Jer
IRF6 polymorphisms in Mexican patients with non-syndromic cleft lip.
Meta gene 2015 Jun 4 8-16.
Ibarra-Arce Aurora, García-Álvarez Martín, Cortés-González Daniel, Ortiz de Zarate-Alarcón Gabriela, Flores-Peña Laura, Sánchez-Camacho Sandra, Arenas-Díaz Silvia, Romero-Valdovinos Mirza, Olivo-Díaz Angéli
Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family.
Genetics research 2015 1 96 e12.
Manjegowda Dinesh S, Prasad Manu, Veerappa Avinash M, Ramachandra Nallur
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
[Clinical and genetic features of Chinese kindreds with Van der Woude syndrome caused by interferon regulatory factor 6 mutation].
Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology 2018 12 36 (6): 623-627.
Du Xin-Ya, Li Xiao-Yu, Wu Bin, Xie Chun, Tian Wei-Do
Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome.
Molecular genetics & genomic medicine 2020 2 8 (5): e1196.
Yu Yanqin, Wan Yatao, Qin Chuanqi, Yue Haitang, Bian Zhuan, He Mi
Screening of IRF6 Variants in Patients Subjected to Genetic Association Studies for Nonsyndromic Cleft Lip/Palate.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2020 Dec 1055665620980238.
Velázquez-Aragón José A, Angel Ariadna González-Del, Alcántara-Ortigoza Miguel A, Reyna-Fabián Miriam E, Estandia-Ortega Bernardet
Association of single nucleotide polymorphisms in the IRF6 gene with nonsyndromic cleft lip with or without cleft palate in Kinh Vietnamese patients.
Molecular biology reports 2022 Dec .
Phan Hoanh Duy Ba, Phuong Lam Hoai, Dang Tran Ngoc, Tram Duong Bich, Vu Hoang A
[Analysis of a Chinese pedigree affected with van der Woude syndrome due to variant of IRF6 gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 11 40 (12): 1517-1520.
Xiangyu Zhu, Peixuan Cao, Yujie Zhu, Jie
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