Pharmacogenomics: the future of drug therapy.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 257, doi. 10.1034/j.1399-0004.2002.620401.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2002 AND VI 62 AND IP 4
Results: 19
1
2
Hereditary motor neuron disease caused by mutations in the ALS2 gene: ‘The long and the short of it’.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 265, doi. 10.1034/j.1399-0004.2002.620402_2.x
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- Publication type:
- Article
3
Autosomal spots that mark the ‘X’.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 266, doi. 10.1034/j.1399-0004.2002.620402_3.x
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- Publication type:
- Article
4
Homologous telomere association of 19q in a female with premature ovarian failure.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 310, doi. 10.1034/j.1399-0004.2002.620410.x
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- Publication type:
- Article
5
Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 321, doi. 10.1034/j.1399-0004.2002.620412.x
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- Publication type:
- Article
6
Analysis of the two common alpha-1-antitrypsin deficiency alleles PiMS and PiMZ as modifiers of Pseudomonas aeruginosa susceptibility in cystic fibrosis.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 325, doi. 10.1034/j.1399-0004.2002.620413.x
- By:
- Publication type:
- Article
7
Association of angiotensin-converting-enzyme gene polymorphism with the depressor response to mild exercise therapy in patients with mild to moderate essential hypertension.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 328, doi. 10.1034/j.1399-0004.2002.620414.x
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- Publication type:
- Article
8
Losing your inhibitions: a mutation in the α1 subunit of the GABA<sub>A</sub> receptor causes autosomal dominant juvenille myoclonic epilepsy.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 268, doi. 10.1034/j.1399-0004.2002.620402_4.x
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- Publication type:
- Article
9
Hair as a diagnostic tool in dysmorphology.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 270, doi. 10.1034/j.1399-0004.2002.620403.x
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- Publication type:
- Article
10
A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 273, doi. 10.1034/j.1399-0004.2002.620404.x
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- Publication type:
- Article
11
Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz–Jeghers syndrome patients.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 282, doi. 10.1034/j.1399-0004.2002.620405.x
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- Publication type:
- Article
12
Germline mutations in the PTEN gene in Israeli patients with Bannayan–Riley–Ruvalcaba syndrome and women with familial breast cancer.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 298, doi. 10.1034/j.1399-0004.2002.620407.x
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- Publication type:
- Article
13
Acute intermittent porphyria in Sweden. Molecular, functional and clinical consequences of some new mutations found in the porphobilinogen deaminase gene.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 288, doi. 10.1034/j.1399-0004.2002.620406.x
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- Publication type:
- Article
14
The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 306, doi. 10.1034/j.1399-0004.2002.620409.x
- By:
- Publication type:
- Article
15
The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 303, doi. 10.1034/j.1399-0004.2002.620408.x
- By:
- Publication type:
- Article
16
A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 334, doi. 10.1034/j.1399-0004.2002.620415.x
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- Publication type:
- Article
17
A 4-Mb critical region for intrauterine growth retardation at 15q26.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 340, doi. 10.1034/j.1399-0004.2002.620416.x
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- Publication type:
- Article
18
A new case of dup(3q) syndrome due to a pure duplication of 3qter.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 4, p. 315, doi. 10.1034/j.1399-0004.2002.620411.x
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- Publication type:
- Article
19
Errata.
- Published in:
- 2002
- Publication type:
- Erratum