The fragile X gene and its function.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 399, doi. 10.1034/j.1399-0004.2001.600601.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2001 AND VI 60 AND IP 6
Results: 15
1
2
When body segmentation goes wrong.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 409, doi. 10.1034/j.1399-0004.2001.600602.x
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- Publication type:
- Article
3
History of genetics through philately – deafness.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 417, doi. 10.1034/j.1399-0004.2001.600603.x
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- Publication type:
- Article
4
A family with a grand-maternally derived interstitial duplication of proximal 15q.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 421, doi. 10.1034/j.1399-0004.2001.600604.x
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- Publication type:
- Article
5
Distribution of α1-antitrypsin PI S and PI Z frequencies in countries outside Europe: a meta-analysis.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 431, doi. 10.1034/j.1399-0004.2001.600605.x
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- Publication type:
- Article
6
To test or not to test: an ethical conflict with presymptomatic testing of individuals at 25% risk for Huntington's disorder.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 442, doi. 10.1034/j.1399-0004.2001.600606.x
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- Publication type:
- Article
7
Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 447, doi. 10.1034/j.1399-0004.2001.600607.x
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- Publication type:
- Article
8
Frequency of the 35delG mutation in the connexin 26 gene in Turkish hearing-impaired patients.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 452, doi. 10.1034/j.1399-0004.2001.600608.x
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- Publication type:
- Article
9
Familial Down syndrome: evidence supporting cytoplasmic inheritance.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 456, doi. 10.1034/j.1399-0004.2001.600609.x
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- Publication type:
- Article
10
A logistic regression model for measuring gene–longevity associations.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 463, doi. 10.1034/j.1399-0004.2001.600610.x
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- Publication type:
- Article
11
Founder mutations in the BRCA1 gene in west Belarusian breast-ovarian cancer families.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 470, doi. 10.1034/j.1399-0004.2001.600611.x
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- Publication type:
- Article
12
Pyruvate kinase deficiency: prevalence of the 1456C→T mutation in the Portuguese population.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 472, doi. 10.1034/j.1399-0004.2001.600612.x
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- Publication type:
- Article
13
Vietnamese sisters with Grebe syndrome on a TV program in Japan.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 474, doi. 10.1034/j.1399-0004.2001.600613.x
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- Publication type:
- Article
14
Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 476, doi. 10.1034/j.1399-0004.2001.600614.x
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- Publication type:
- Article
15
A systematic search for single nucleotide polymorphisms (SNPs) in the insulin receptor gene: association of an SNP with hyperlipidemia in Japanese type 2 diabetic subjects.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 479, doi. 10.1034/j.1399-0004.2001.600615.x
- By:
- Publication type:
- Article