Testing all possible protein–protein interactions in yeast.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 350, doi. 10.1034/j.1399-0004.2000.580503.3.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2000 AND VI 58 AND IP 5
Results: 17
1
2
Insights into the pathogenesis of neurofibromatosis 1 vasculopathy.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 341, doi. 10.1034/j.1399-0004.2000.580501.x
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- Publication type:
- Article
3
The vasculopathy of NF1 and histogenesis control genes.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 345, doi. 10.1034/j.1399-0004.2000.580502.x
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- Publication type:
- Article
4
Huntington's disease on a GeneChip.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 348, doi. 10.1034/j.1399-0004.2000.580503.1.x
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- Publication type:
- Article
5
A glutamine-rich protein involved in Notch signalling.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 349, doi. 10.1034/j.1399-0004.2000.580503.2.x
- By:
- Publication type:
- Article
6
The causes and consequences of random and non-random X chromosome inactivation in humans.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 353, doi. 10.1034/j.1399-0004.2000.580504.x
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- Publication type:
- Article
7
Hugo Ethics Committee statement on benefit sharing.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 364, doi. 10.1034/j.1399-0004.2000.580505.x
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- Publication type:
- Article
8
Benefit-sharing and other protections for communities in genetic research.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 367, doi. 10.1034/j.1399-0004.2000.580506.x
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- Publication type:
- Article
9
The common mutations in the lipoprotein lipase gene in Italy: effects on plasma lipids and angiographically assessed coronary atherosclerosis.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 369, doi. 10.1034/j.1399-0004.2000.580507.x
- By:
- Publication type:
- Article
10
A multivariate analysis of 59 candidate genes in personality traits: the temperament and character inventory.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 375, doi. 10.1034/j.1399-0004.2000.580508.x
- By:
- Publication type:
- Article
11
Sudden death caused by pulmonary thromboembolism in Proteus syndrome.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 386, doi. 10.1034/j.1399-0004.2000.580509.x
- By:
- Publication type:
- Article
12
Kyphomelic dysplasia: a rare form of semilethal skeletal dysplasia.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 390, doi. 10.1034/j.1399-0004.2000.580510.x
- By:
- Publication type:
- Article
13
Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 396, doi. 10.1034/j.1399-0004.2000.580511.x
- By:
- Publication type:
- Article
14
Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian children.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 403, doi. 10.1034/j.1399-0004.2000.580512.x
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- Publication type:
- Article
15
The frequency of the C677T substitution in the methylenetetrahydrofolate reductase gene in Manitoba.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 406, doi. 10.1034/j.1399-0004.2000.580513.x
- By:
- Publication type:
- Article
16
Glycogen storage disease type Ia and Sanfilippo syndrome type B in a patient with a balanced translocation.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 409, doi. 10.1034/j.1399-0004.2000.580514.x
- By:
- Publication type:
- Article
17
Familial amyloid polyneuropathy in a Spanish family with a transthyretin deletion (ΔVal 122) presenting with carpal tunnel syndrome.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 5, p. 411, doi. 10.1034/j.1399-0004.2000.580515.x
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- Publication type:
- Article