Sibship stability of genotype and phenotype in myotonic dystrophy.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 220, doi. 10.1034/j.1399-0004.2002.620306.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2002 AND VI 62 AND IP 3
Results: 14
1
2
Hotspots.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 191, doi. 10.1034/j.1399-0004.2001.620301.x
- By:
- Publication type:
- Article
3
Developing a quality scoring system for epidemiological surveys of genetic disorders.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 230, doi. 10.1034/j.1399-0004.2002.620308.x
- By:
- Publication type:
- Article
4
Apolipoprotein molecular variation in Moroccan Berbers: pentanucleotide (TTTTA)n repeat in the LPA gene and APOE-C1-C2 gene cluster.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 240, doi. 10.1034/j.1399-0004.2002.620310.x
- By:
- Publication type:
- Article
5
Normal levels of soluble transferrin receptor in Friedreich ataxia.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 250, doi. 10.1034/j.1399-0004.2002.620312.x
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- Publication type:
- Article
6
Novel neuropeptide Y1 and Y5 receptor gene variants: associations with serum triglyceride and high-density lipoprotein cholesterol levels.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 196, doi. 10.1034/j.1399-0004.2002.620302.x
- By:
- Publication type:
- Article
7
Genotyping of Israeli infertile men with idiopathic oligozoospermia.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 203, doi. 10.1034/j.1399-0004.2002.620303.x
- By:
- Publication type:
- Article
8
Genetic polymorphisms of the apolipoprotein A-IV in a Greek population and their relation to plasma lipid and lipoprotein levels.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 208, doi. 10.1034/j.1399-0004.2002.620304.x
- By:
- Publication type:
- Article
9
Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q11.2 deletion.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 214, doi. 10.1034/j.1399-0004.2002.620305.x
- By:
- Publication type:
- Article
10
Comparison of two different protocols of neonatal screening for cystic fibrosis.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 245, doi. 10.1034/j.1399-0004.2002.620311.x
- By:
- Publication type:
- Article
11
ATP binding cassette G5 C1950G polymorphism may affect blood cholesterol concentrations in humans.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 226, doi. 10.1034/j.1399-0004.2002.620307.x
- By:
- Publication type:
- Article
12
Familial hypocalciuric hypercalcaemia in a large family with neurofibromatosis 1.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 252, doi. 10.1034/j.1399-0004.2002.620313.x
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- Publication type:
- Article
13
Lack of association between methylenetetrahydrofolate reductase (MTHFR) C677T and ischaemic heart disease (IHD): family-based association study in a Spanish population.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 235, doi. 10.1034/j.1399-0004.2002.620309.x
- By:
- Publication type:
- Article
14
A novel mutation (N32K) of GLUT2 gene in a Japanese patient with Fanconi–Bickel syndrome.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 3, p. 255, doi. 10.1034/j.1399-0004.2002.620314.x
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- Publication type:
- Article