Found: 16
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Influence of the angiotensin-converting enzyme gene insertion/deletion polymorphism on lipoprotein/lipid response to gemfibrozil.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 1, p. 45, doi. 10.1034/j.1399-0004.2002.620106.x
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- Article
Two more genes involved in recental retardation in an ever x-panding repertoire of proteins and pathways.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 24, doi. 10.1034/j.1399-0004.2002.6201031.x
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- Article
Non-syndromic autosomal-dominant deafness.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 1, doi. 10.1034/j.1399-0004.2002.620101.x
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- Article
Novel skeletal muscle ryanodine receptor mutation in a large Brazilian family with malignant hyperthermia.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 80, doi. 10.1034/j.1399-0004.2002.620111.x
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- Article
Apolipoprotein E gene polymorphism in cerebrovascular disease: a case–controlstudy.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 39, doi. 10.1034/j.1399-0004.2002.620105.x
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- Article
Re-engineering dystrophin for gene therapy of Duchenne muscular dystrophy.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 25, doi. 10.1034/j.1399-0004.2002.610403_2.x
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- Article
Development and diseases of the pancreas.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 14, doi. 10.1034/j.1399-0004.2002.620102.x
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- Article
The relationship between plasma t-PA and PAI-1 levels is dependent on epistatic effects of the ACE I/D and PAI-1 4G/5G polymorphisms.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 53, doi. 10.1034/j.1399-0004.2002.620107.x
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- Article
Service provision of complex mutation analysis: a technical and economic appraisal using dystrophin point mutation analysis as an example.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 29, doi. 10.1034/j.1399-0004.2002.620104.x
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- Article
Towards an understanding of the molecular pathogenesis of autosomal-recessive polycystic kidney disease (ARPKD): identification of a novel protein, fibrocystin.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 27, doi. 10.1034/j.1399-0004.2002.6201033.x
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- Article
657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 84, doi. 10.1034/j.1399-0004.2002.620112.x
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- Article
Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 89, doi. 10.1034/j.1399-0004.2002.620113.x
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- Article
Mutations in the X-linked spondyloepiphyseal dysplasia tarda (SEDL) coding sequence are not a common cause of early primary osteoarthritis in men.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 94, doi. 10.1034/j.1399-0004.2002.620114.x
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- Article
Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection system.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 60, doi. 10.1034/j.1399-0004.2002.620108.x
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- Article
DGAT1 promoter polymorphism associated with alterations in body mass index, high density lipoprotein levels and blood pressure in Turkish women.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 68, doi. 10.1034/j.1399-0004.2002.620109.x
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- Publication type:
- Article
A comparison of combinatorial partitioning and linear regression for the detection of epistatic effects of the ACE I/D and PAI-1 4G/5G polymorphisms on plasma PAI-1 levels.
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- Clinical Genetics, 2002, v. 62, n. 1, p. 74, doi. 10.1034/j.1399-0004.2002.620110.x
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- Publication type:
- Article