Contribution of Gender-Specific Genetic Factors to Osteoporosis Risk.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 696, doi. 10.1111/j.1469-1809.2008.00447.x
- By:
- Publication type:
- Article
Works matching IS 00034800 AND DT 2008 AND VI 72 AND IP 5
Results: 16
1
2
Cognitive Functioning and Survival in the Elderly: The SSADH C538T Polymorphism.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 630, doi. 10.1111/j.1469-1809.2008.00450.x
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- Publication type:
- Article
3
Correlation Analyses Reveal a Substantial Influence of Allelic Gaps on the Investigation of Genetic Diversity of Modern Human Populations with Microsatellites.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 644, doi. 10.1111/j.1469-1809.2008.00445.x
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- Publication type:
- Article
4
Genetic Epidemiology of Subclinical Cardiovascular Disease in the Diabetes Heart Study.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 598, doi. 10.1111/j.1469-1809.2008.00446.x
- By:
- Publication type:
- Article
5
Identifying Modifier Loci in Existing Genome Scan Data.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 670, doi. 10.1111/j.1469-1809.2008.00449.x
- By:
- Publication type:
- Article
6
Quantification of the Genetic Component of Basal C-Reactive Protein Expression in SLE Nuclear Families.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 611, doi. 10.1111/j.1469-1809.2008.00444.x
- By:
- Publication type:
- Article
7
Exact Trait-Model-Free Tests for Linkage Detection in Pedigrees.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 676, doi. 10.1111/j.1469-1809.2008.00451.x
- By:
- Publication type:
- Article
8
A Genome-wide Scan in an Amish Pedigree with Parkinsonism.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 621, doi. 10.1111/j.1469-1809.2008.00452.x
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- Publication type:
- Article
9
On the asymptotic equivalence of allelic and trend statistic under Hardy-Weinberg equilibrium.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 589, doi. 10.1111/j.1469-1809.2008.00453.x
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- Publication type:
- Article
10
Four SNPS on Chromosome 9p21 Confer Risk to Premature, Familial CAD and MI in an American Caucasian Population (GeneQuest).
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 654, doi. 10.1111/j.1469-1809.2008.00454.x
- By:
- Publication type:
- Article
11
Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot-Marie-Tooth Subtype CMT2B1 in Families from North Western Africa.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 590, doi. 10.1111/j.1469-1809.2008.00456.x
- By:
- Publication type:
- Article
12
Identification of Association of Common AGGF1 Variants with Susceptibility for Klippel-Trenaunay Syndrome Using the Structure Association Program.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 636, doi. 10.1111/j.1469-1809.2008.00458.x
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- Publication type:
- Article
13
Erratum.
- Published in:
- 2008
- Publication type:
- Correction Notice
14
European Mathematical Genetics Meeting, Rotterdam, the Netherlands, 10<sup>th</sup>–11<sup>th</sup> April 2008.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 687, doi. 10.1111/j.1469-1809.2008.00461.x
- Publication type:
- Article
15
HMBS Mutations in Chinese Patients with Acute Intermittent Porphyria.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 683, doi. 10.1111/j.1469-1809.2008.00463.x
- By:
- Publication type:
- Article
16
A Bayesian Spatial Multimarker Genetic Random-Effect Model for Fine-Scale Mapping.
- Published in:
- Annals of Human Genetics, 2008, v. 72, n. 5, p. 658, doi. 10.1111/j.1469-1809.2008.00459.x
- By:
- Publication type:
- Article