Works matching IS 03406717 AND DT 2007 AND VI 121 AND IP 3/4
Results: 26
AZFc somatic microdeletions and copy number polymorphism of the DAZ genes in human males exposed to natural background radiation.
- Published in:
- Human Genetics, 2007, v. 121, n. 3/4, p. 337, doi. 10.1007/s00439-006-0318-7
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- Article
An entropy-based genome-wide transmission/disequilibrium test.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 357, doi. 10.1007/s00439-007-0322-6
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- Article
Enrichment of longevity phenotype in mtDNA haplogroups D4b2b, D4a, and D5 in the Japanese population.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 347, doi. 10.1007/s00439-007-0330-6
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- Article
Common variation in KLKB1 and essential hypertension risk: tagging-SNP haplotype analysis in a case-control study.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 327, doi. 10.1007/s00439-007-0340-4
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- Article
Candidate SNPs for a universal individual identification panel.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 305, doi. 10.1007/s00439-007-0342-2
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- Article
A mutation in the lipase H ( LIPH) gene underlie autosomal recessive hypotrichosis.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 319, doi. 10.1007/s00439-007-0344-0
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- Article
Cholesteryl ester transfer protein gene haplotypes, plasma high-density lipoprotein levels and the risk of coronary heart disease.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 401, doi. 10.1007/s00439-007-0326-2
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- Article
Identification of 54 large deletions/duplications in TSC1 and TSC2 using MLPA, and genotype-phenotype correlations.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 389, doi. 10.1007/s00439-006-0308-9
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- Article
SP110 polymorphisms are not associated with pulmonary tuberculosis in a South African population.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 521, doi. 10.1007/s00439-007-0335-1
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- Article
Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 377, doi. 10.1007/s00439-007-0333-3
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- Publication type:
- Article
Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndrome.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 369, doi. 10.1007/s00439-007-0336-0
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- Publication type:
- Article
Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study.
- Published in:
- Human Genetics, 2007, v. 121, n. 3/4, p. 511, doi. 10.1007/s00439-006-0312-0
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- Publication type:
- Article
Mutations in autism susceptibility candidate 2 ( AUTS2) in patients with mental retardation.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 501, doi. 10.1007/s00439-006-0284-0
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- Article
Announcement.
- Published in:
- Human Genetics, 2007, v. 121, n. 3/4, p. 527, doi. 10.1007/s00439-007-0346-y
- Publication type:
- Article
M. K. Raizada, J. F. R. Paton, S. Kasparov, M. J. Katovich (eds): Cardiovascular genomics.
- Published in:
- 2007
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- Publication type:
- Book Review
Autosomal recessive juvenile onset cataract associated with mutation in BFSP1.
- Published in:
- Human Genetics, 2007, v. 121, n. 3/4, p. 475, doi. 10.1007/s00439-006-0319-6
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- Publication type:
- Article
The physical phenotype of girls and women with Turner syndrome is not X-imprinted.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 469, doi. 10.1007/s00439-007-0324-4
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- Publication type:
- Article
The advantages of dense marker sets for linkage analysis with very large families.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 459, doi. 10.1007/s00439-007-0323-5
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- Publication type:
- Article
Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 451, doi. 10.1007/s00439-006-0317-8
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- Publication type:
- Article
Epigenetic control of the critical region for premature ovarian failure on autosomal genes translocated to the X chromosome: a hypothesis.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 441, doi. 10.1007/s00439-007-0329-z
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- Article
Achromatopsia: the CNGB3 p.T383fsX mutation results from a founder effect and is responsible for the visual phenotype in the original report of uniparental disomy 14.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 433, doi. 10.1007/s00439-006-0314-y
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- Article
Quantitative effects of common genetic variations in the 3′UTR of the human LDL-receptor gene and their associations with plasma lipid levels in the Atherosclerosis Risk in Communities study.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 421, doi. 10.1007/s00439-007-0327-1
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- Publication type:
- Article
A novel locus for autosomal recessive spastic ataxia on chromosome 17p.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 413, doi. 10.1007/s00439-007-0328-0
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- Publication type:
- Article
CYP19A1 polymorphisms are associated with bone mineral density in Chinese men.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 491, doi. 10.1007/s00439-006-0303-1
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- Publication type:
- Article
Genetic variation in tumor necrosis factor and lymphotoxin-alpha ( TNF–LTA) and breast cancer risk.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 483, doi. 10.1007/s00439-006-0315-x
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- Article
Edwin K. Silverman, Steven D. Shapiro, David A. Lomas, Scott T. Weiss: Respiratory Genetics.
- Published in:
- 2007
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- Publication type:
- Book Review