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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 8, 2024. (Total: 233355Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Neural Tube Defects and VANGL2[original query]
VANGL2 mutations in human cranial neural-tube defects.
The New England journal of medicine 2010 Jun 362 (23): 2232-5.
Lei Yun-Ping, Zhang Ting, Li Hong, Wu Bai-Lin, Jin Li, Wang Hong-Y
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
Identification of novel CELSR1 mutations in spina bifida.
PloS one 2014 9 (3): e92207.
Lei Yunping, Zhu Huiping, Yang Wei, Ross M Elizabeth, Shaw Gary M, Finnell Richard
Role of the planar cell polarity gene Protein tyrosine kinase 7 in neural tube defects in humans.
Birth defects research. Part A, Clinical and molecular teratology 2015 Sep .
Wang Mingqin, De Marco Patrizia, Merello Elisa, Drapeau Pierre, Capra Valeria, Kibar Zo
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
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