Apolipoprotein B-100 gene Xba I polymorphism and cholesterol gallstone disease.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 304, doi. 10.1034/j.1399-0004.2000.570410.x
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- Publication type:
- Article
Works matching IS 00099163 AND DT 2000 AND VI 57 AND IP 4
Results: 14
1
2
Mouse models for human disease.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 237, doi. 10.1034/j.1399-0004.2000.570401.x
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- Publication type:
- Article
3
Mutated presenilins and Alzheimer's disease: the culprit could be calcium signaling.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 245, doi. 10.1034/j.1399-0004.2000.570402.x
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- Publication type:
- Article
4
Affective disorders: susceptibility and drug efficacy may be determined by the serotonin transporter promoter polymorphism.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 247, doi. 10.1034/j.1399-0004.2000.570402.1.x
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- Publication type:
- Article
5
Physical activity: good for your health, very good for your gene expression.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 249, doi. 10.1034/j.1399-0004.2000.570402.2.x
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- Publication type:
- Article
6
Online Mendelian Inheritance in Man (OMIM) as a knowledgebase for human developmental disorders.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 253, doi. 10.1034/j.1399-0004.2000.570403.x
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- Publication type:
- Article
7
Genetic landmarks through philately – Karl Landsteiner: the father of blood grouping.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 267, doi. 10.1034/j.1399-0004.2000.570404.x
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- Publication type:
- Article
8
Gender-specific effects of NAT2 and GSTM1 in bladder cancer.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 270, doi. 10.1034/j.1399-0004.2000.570405.x
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- Publication type:
- Article
9
Localization of an acromesomelic dysplasia on chromosome 9 by homozygosity mapping.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 278, doi. 10.1034/j.1399-0004.2000.570406.x
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- Publication type:
- Article
10
Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel ‘hot spot’ in codon 47.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 284, doi. 10.1034/j.1399-0004.2000.570407.x
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- Publication type:
- Article
11
Molecular analysis of Y chromosome long arm structural instability in patients with gonadal dysfunction.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 291, doi. 10.1034/j.1399-0004.2000.570408.x
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- Publication type:
- Article
12
Association of the R485K polymorphism of the Factor V gene with poor response to activated protein C and increased risk of coronary artery disease in the Chinese population.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 296, doi. 10.1034/j.1399-0004.2000.570409.x
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- Publication type:
- Article
13
Relation between the insertion/deletion polymorphism in the gene coding for receptor associated protein (RAP) and plasma apolipoprotein AI (apoAI) and high-density lipoprotein cholesterol (HDL) levels.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 309, doi. 10.1034/j.1399-0004.2000.570411.x
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- Publication type:
- Article
14
Identification of a novel frameshift β-thalassemia mutation in an Asian Indian.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 4, p. 311, doi. 10.1034/j.1399-0004.2000.570412.x
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- Publication type:
- Article