Works matching IS 14345161 AND DT 2013 AND VI 58 AND IP 1
Results: 12
Genotype instability during long-term subculture of lymphoblastoid cell lines.
- Published in:
- Journal of Human Genetics, 2013, v. 58, n. 1, p. 16, doi. 10.1038/jhg.2012.123
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- Article
Huntington disease-like 2 (HDL2) in Venezuela: frequency and ethnic origin.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 3, doi. 10.1038/jhg.2012.111
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- Article
Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 33, doi. 10.1038/jhg.2012.131
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- Article
Protein tyrosine phosphatase receptor-like genes are frequently hypermethylated in sporadic colorectal cancer.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 11, doi. 10.1038/jhg.2012.119
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- Article
New year wishes and updates.
- Published in:
- Journal of Human Genetics, 2013, v. 58, n. 1, p. 1, doi. 10.1038/jhg.2012.136
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- Article
Use of alternative promoters may hide genetic effects on phenotypic traits.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 47, doi. 10.1038/jhg.2012.115
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- Article
Interaction of C1GALT1-IL5RA on the susceptibility to IgA nephropathy in Southern Han Chinese.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 40, doi. 10.1038/jhg.2012.133
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- Article
Impact of four loci on serum tamsulosin hydrochloride concentration.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 21, doi. 10.1038/jhg.2012.126
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- Article
HOX gene methylation status analysis in patients with hereditary breast cancer.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 51, doi. 10.1038/jhg.2012.118
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- Article
Strong influence of variants near MC4R on adiposity in children and adults: a cross-sectional study in Indian population.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 27, doi. 10.1038/jhg.2012.129
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- Article
Constructing a contemporary gene-environmental cohort: study design of the Yamagata Molecular Epidemiological Cohort Study.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 54, doi. 10.1038/jhg.2012.128
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- Article
Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding.
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- Journal of Human Genetics, 2013, v. 58, n. 1, p. 7, doi. 10.1038/jhg.2012.116
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- Article