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Molecular Screening of VAX1 Gene Polymorphisms Uncovered the Genetic Heterogeneity of Nonsyndromic Orofacial Cleft Among Saudi Arabian Patients

机译：vax1基因多态性的分子筛发现了沙特阿拉伯患者中非肌瘤肉体裂缝的遗传异质性

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Heba Jafar Sabbagh; Nicola P.T. Innes; Sherif Edris Ahmed; Azeez Butali; Eman Abdulbaset Alnamnakani; Sari M. Rabah; Mustafa A. Hamdan; Nasir H. Alhamlan; Fatma Dawood Abdulhameed; Mona Hassan Ahmed Hassan; Hadiah Bassam Al Mahdi; Najlaa M. Alamoudi; Jumana Y. Al-Aama; Sumer M. Alaki; Peter A. Mossey;
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1. Polymorphisms in FGF12 , VCL , CX43 and VAX1 in Brazilian patients with nonsyndromic cleft lip with or without cleft palate [J] . Sibele Nascimento de Aquino, Ana Camila Messetti, Elizabete Bagordakis, BMC Medical Genetics . 2013,第1期

机译：巴西非综合征性唇裂伴或不伴c裂患者FGF12，VCL，CX43和VAX1的多态性
2. Environmental Risk Factors in the Etiology of Nonsyndromic Orofacial Clefts in the Western Region of Saudi Arabia. [J] . Heba J Sabbagh, Najlaa M Alamoudi, Fatma Dawood Abdulhameed, The Cleft palate-craniofacial journal: official publication of the American Cleft Palate-Craniofacial Association . 2016,第4期

机译：沙特阿拉伯西部非综合征性口面部裂痕病因的环境危险因素。
3. VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of a VAX1 phenotype in humans [J] . SlavotinekA.M., ChaoR., VacikT., Human mutation . 2012,第2期

机译：与小眼症，call体发育不全和口面部裂伤相关的VAX1突变：人类中VAX1表型的第一个描述
4. Evaluation of fetal and maternal genetic effects on the risk of isolated orofacial clefts [C] . A Jugessur, M Shi 2, HK Gjessing 3, International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies . 2009

机译：对胎儿和母体遗传效应的评价对孤立的orofacial裂缝的风险
5. High-throughput genetic association study on candidate genes for nonsyndromic oral clefts. [D] . Park, Ji Wan. 2006

机译：非综合征性口腔裂的候选基因的高通量遗传关联研究。
6. Polymorphisms in FGF12 VCL CX43 and VAX1 in Brazilian patients with nonsyndromic cleft lip with or without cleft palate [O] . Sibele Nascimento de Aquino, Ana Camila Messetti, Elizabete Bagordakis, 2013

机译：巴西非综合征性唇裂伴或不伴c裂患者FGF12VCLCX43和VAX1的多态性
7. Polymorphisms in FGF12, VCL, CX43 and VAX1 in Brazilian patients with nonsyndromic cleft lip with or without cleft palate [O] . de Aquino, SN, Messetti, AC, Bagordakis, E, 2015

机译：巴西非综合征性唇裂伴或不伴c裂患者FGF12，VCL，CX43和VAX1的多态性

Molecular Screening of VAX1 Gene Polymorphisms Uncovered the Genetic Heterogeneity of Nonsyndromic Orofacial Cleft Among Saudi Arabian Patients

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