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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Human Genome Epidemiology Literature Finder|Home|PHGKB
Human Genome Epidemiology Literature Finder
Last data update: Feb 8, 2024
. (Total: 225926Documents)
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LEFTY1[original query]
Characterization of nodal/TGF-lefty signaling pathway gene variants for possible roles in congenital heart diseases.
PloS one 2014 9 (8): e104535.
Deng Xia, Zhou Jing, Li Fei-Feng, Yan Peng, Zhao Er-Ying, Hao Ling, Yu Kai-Jiang, Liu Shu-L
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Exploratory genotype-phenotype correlations of facial form and asymmetry in unaffected relatives of children with non-syndromic cleft lip and/or palate.
Journal of anatomy 2014 Jun 224 (6): 688-709.
Miller Steven F, Weinberg Seth M, Nidey Nichole L, Defay David K, Marazita Mary L, Wehby George L, Moreno Uribe Lina
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[Identification of mutations associated with coronary artery lesion susceptibility in Kawasaki disease by targeted enrichment of genomic region sequencing technique].
Zhonghua er ke za zhi = Chinese journal of pediatrics 2017 Jul 55 (7): 529-533.
Zhu D Y, Song S R, Xie L J, Qiu F, Yang J, Xiao T T, Huang
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Association of maternal hypertension and diabetes with variants of the NKX2-5, LEFTY1 and LEFTY2 genes in children with congenital heart defects: a case-control study from Pakistani Population.
Molecular biology reports 2023 4 .
Sana Ashiq, Muhammad Farooq Sab
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Page last reviewed:
Feb 1, 2024
Page last updated:
Mar 25, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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