Found: 18
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The Finnish disease heritage III: the individual diseases.
- Published in:
- Human Genetics, 2003, v. 112, n. 5/6, p. 470, doi. 10.1007/s00439-002-0877-1
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- Article
Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 610, doi. 10.1007/s00439-003-0937-1
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- Article
Finnish Disease Heritage II: population prehistory and genetic roots of Finns.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 457, doi. 10.1007/s00439-002-0876-2
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- Article
Genome-wide targeted search for human specific and polymorphic L1 integrations.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 527, doi. 10.1007/s00439-002-0904-2
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- Article
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 573, doi. 10.1007/s00439-003-0917-5
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- Article
Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol.
- Published in:
- Human Genetics, 2003, v. 112, n. 5/6, p. 552, doi. 10.1007/s00439-002-0893-1
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- Article
European Academy of Andrology (EAA) International Symposium.
- Published in:
- Human Genetics, 2003, v. 112, n. 5/6, p. 623, doi. 10.1007/s00439-003-0947-z
- Publication type:
- Article
Finnish Disease Heritage I:.
- Published in:
- Human Genetics, 2003, v. 112, n. 5/6, p. 441, doi. 10.1007/s00439-002-0875-3
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- Article
Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndrome.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 563, doi. 10.1007/s00439-002-0884-2
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- Article
Prediction of clinical outcome with microarray data: a partial least squares discriminant analysis (PLS-DA) approach.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 581, doi. 10.1007/s00439-003-0921-9
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- Article
Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 534, doi. 10.1007/s00439-002-0899-8
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- Article
G. Evers-Kiebooms, M.W. Zoeteweij, P.S. Harper (eds): Prenatal testing for late onset neurogenetic diseases: BIOS Scientific (ISBN 1-8599-6019-7).
- Published in:
- 2003
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- Publication type:
- Book Review
Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 593, doi. 10.1007/s00439-002-0905-1
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- Article
Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 542, doi. 10.1007/s00439-003-0908-6
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- Article
Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 567, doi. 10.1007/s00439-003-0911-y
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- Article
A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 600, doi. 10.1007/s00439-003-0910-z
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- Publication type:
- Article
Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 619, doi. 10.1007/s00439-003-0939-z
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- Article
No evidence of fetal DNA persistence in maternal plasma after pregnancy.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 617, doi. 10.1007/s00439-003-0919-3
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- Article