Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 3, p. 176, doi. 10.1038/jhg.2011.148
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- Publication type:
- Article
Works matching IS 14345161 AND DT 2012 AND VI 57 AND IP 3
Results: 15
1
2
Common genetic factors for hematological traits in Humans.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 3, p. 161, doi. 10.1038/jhg.2012.2
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- Publication type:
- Article
3
Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion.
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- Journal of Human Genetics, 2012, v. 57, n. 3, p. 191, doi. 10.1038/jhg.2011.154
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- Article
4
Myotonic dystrophy type 2 is rare in the Japanese population.
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- Journal of Human Genetics, 2012, v. 57, n. 3, p. 219, doi. 10.1038/jhg.2011.152
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- Publication type:
- Article
5
Commentary on the mutation spectrum of and founder effects affecting the PTS gene in East-Asian populations.
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- Journal of Human Genetics, 2012, v. 57, n. 3, p. 159, doi. 10.1038/jhg.2011.153
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- Publication type:
- Article
6
A commentary on Association of adiponectin polymorphism with cord blood adiponectin concentrations and intrauterine growth.
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- Journal of Human Genetics, 2012, v. 57, n. 3, p. 157, doi. 10.1038/jhg.2011.149
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- Publication type:
- Article
7
A family of oculofaciocardiodental syndrome (OFCD) with a novel BCOR mutation and genomic rearrangements involving NHS.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 3, p. 197, doi. 10.1038/jhg.2012.4
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- Publication type:
- Article
8
Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 3, p. 202, doi. 10.1038/jhg.2012.5
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- Publication type:
- Article
9
Present Y chromosomes reveal the ancestry of Emperor CAO Cao of 1800 years ago.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 3, p. 216, doi. 10.1038/jhg.2011.147
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- Publication type:
- Article
10
Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.
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- Journal of Human Genetics, 2012, v. 57, n. 3, p. 170, doi. 10.1038/jhg.2011.122
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- Publication type:
- Article
11
Spectra of BRCA1 and BRCA2 mutations in Korean patients with breast cancer: the importance of whole-gene sequencing.
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- Journal of Human Genetics, 2012, v. 57, n. 3, p. 222, doi. 10.1038/jhg.2012.13
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- Publication type:
- Article
12
Spectra of BRCA1 and BRCA2 mutations in Korean patients with breast cancer: the importance of whole-gene sequencing.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 3, p. 212, doi. 10.1038/jhg.2011.139
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- Publication type:
- Article
13
Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 3, p. 221, doi. 10.1038/jhg.2012.3
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- Publication type:
- Article
14
Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 3, p. 207, doi. 10.1038/jhg.2012.7
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- Publication type:
- Article
15
Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 3, p. 184, doi. 10.1038/jhg.2011.150
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- Publication type:
- Article