A Family-Based Robust Multivariate Association Test Using Maximum Statistic.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 117, doi. 10.1111/ahg.12054
- By:
- Publication type:
- Article
Works matching IS 00034800 AND DT 2014 AND VI 78 AND IP 2
Results: 7
1
2
A DFNA5 Mutation Identified in Japanese Families with Autosomal Dominant Hereditary Hearing Loss.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 83, doi. 10.1111/ahg.12053
- By:
- Publication type:
- Article
3
Mutational Spectrum of the C1 Inhibitor Gene in a Cohort of Italian Patients with Hereditary Angioedema: Description of Nine Novel Mutations.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 73, doi. 10.1111/ahg.12052
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- Publication type:
- Article
4
Nonparametric Tests of Associations with Disease Based on U-Statistics.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 141, doi. 10.1111/ahg.12049
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- Publication type:
- Article
5
Utilising Family-Based Designs for Detecting Rare Variant Disease Associations.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 129, doi. 10.1111/ahg.12051
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- Publication type:
- Article
6
Tumor Necrosis Factor and Interleukin-6 Gene Polymorphisms and Endometriosis Risk in Asians: A Systematic Review and Meta-Analysis.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 104, doi. 10.1111/ahg.12048
- By:
- Publication type:
- Article
7
Recent Radiation within Y-chromosomal Haplogroup R-M269 Resulted in High Y-STR Haplotype Resemblance.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 92, doi. 10.1111/ahg.12050
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- Publication type:
- Article