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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 - 7 (of 7 Records)

Query Trace: Neural Tube Defects and VANGL1[original query]
Novel mutations in VANGL1 in neural tube defects.
Human mutation 2009 Mar .
Kibar Z, Bosoi CM, Kooistra M, Salem S, Finnell RH, De Marco P, Merello E, Bassuk AG, Capra V, Gros P
VANGL1 rare variants associated with neural tube defects affect convergent extension in zebrafish.
Mechanisms of development 2010 1 127 (7-8): 385-92.
Reynolds Annie, McDearmid Jonathan R, Lachance Stephanie, De Marco Patrizia, Merello Elisa, Capra Valeria, Gros Philippe, Drapeau Pierre, Kibar Zo
Expanding the mutational spectrum associated to neural tube defects: literature revision and description of novel VANGL1 mutations.
Birth defects research. Part A, Clinical and molecular teratology 2015 Jan 103 (1): 51-61.
Merello E, Mascelli S, Raso A, Piatelli G, Consales A, Cama A, Kibar Z, Capra V, Marco Patrizia
Association between VANGL1 gene polymorphisms and neural tube defects.
Neuropediatrics 2014 Aug 45 (4): 234-9.
Cai Chunquan, Shi Ouyan, Wang Baiqi, Chang Baoxing, Yang Rui, Wang Yinsong, Wang Fang, Shen Changho
Digenic variants of planar cell polarity genes in human neural tube defect patients.
Molecular genetics and metabolism 2018 3 124 (1): 94-100.
Wang Linlin, Xiao Yanhui, Tian Tian, Jin Lei, Lei Yunping, Finnell Richard H, Ren Aig
Rare copy number variations of planar cell polarity genes are associated with human neural tube defects.
Neurogenetics 2020 May .
Tian Tian, Lei Yunping, Chen Yongyan, Guo Yinnan, Jin Lei, Finnell Richard H, Wang Linlin, Ren Aig
Single nucleotide polymorphisms of PCP pathway related genes participate in the occurrence and development of neural tube defect.
Molecular genetics & genomic medicine 2022 11 11 (1): e2094.
Liu Yan, Dong Liang, Zhi Xiufang, Liu Yang, Zhao Linsheng, Xu Xiaowei, Wang Lu, Zheng Jie, Pu Linjie, Gu Chunyu, Shu Jianbo, Cai Chunqu
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