A patient with treatment-resistant schizophrenia and cytochrome P4502D6 gene duplication.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 152, doi. 10.1034/j.1399-0004.2002.610211.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2002 AND VI 61 AND IP 2
Results: 17
1
2
A low prevalence of the C677T mutation in the methylenetetrahydrofolate reductase gene in Asian Indians.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 155, doi. 10.1034/j.1399-0004.2002.610212.x
- By:
- Publication type:
- Article
3
Exclusion of candidate gene loci for adult onset primary open-angle glaucoma in a genetically isolated population.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 160, doi. 10.1034/j.1399-0004.2002.610213.x
- By:
- Publication type:
- Article
4
The complexities of ocular genetics.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 79, doi. 10.1034/j.1399-0004.2002.610201.x
- By:
- Publication type:
- Article
5
Table of Contents.
- Published in:
- 2002
- Publication type:
- Table of Contents
6
Genetic control of caudal development.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 89, doi. 10.1034/j.1399-0004.2002.610202.x
- By:
- Publication type:
- Article
7
Communicating a new gene vital for speech and language.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 97, doi. 10.1034/j.1399-0004.2002.610203.x
- By:
- Publication type:
- Article
8
Acanthocytosis in a patient with homozygous familial hypobetalipoproteinemia due to a novel APOB splice site mutation.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 101, doi. 10.1034/j.1399-0004.2002.610204.x
- By:
- Publication type:
- Article
9
ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 115, doi. 10.1034/j.1399-0004.2002.610206.x
- By:
- Publication type:
- Article
10
Participation rates of Ashkenazi Jews in a colon cancer community-based screening/prevention study.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 104, doi. 10.1034/j.1399-0004.2002.610205.x
- By:
- Publication type:
- Article
11
The effect of six polymorphisms in the Apolipoprotein B gene on parameters of lipid metabolism in a Danish population.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 126, doi. 10.1034/j.1399-0004.2002.610207.x
- By:
- Publication type:
- Article
12
A CGH study of 27 patients with CHARGE association.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 135, doi. 10.1034/j.1399-0004.2002.610208.x
- By:
- Publication type:
- Article
13
Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 139, doi. 10.1034/j.1399-0004.2002.610209.x
- By:
- Publication type:
- Article
14
RMRP gene sequence analysis confirms a cartilage-hair hypoplasia variant with only skeletal manifestations and reveals a high density of single-nucleotide polymorphisms.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 146, doi. 10.1034/j.1399-0004.2002.610210.x
- By:
- Publication type:
- Article
15
Molecular cytogenetic analysis of a Xp21.3-pter deletion in a family with normal and short stature.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 163, doi. 10.1034/j.1399-0004.2002.610214.x
- By:
- Publication type:
- Article
16
Developmental Genome Anatomy Project (DGAP).
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 166, doi. 10.1034/j.1399-0004.2002.610215.x
- Publication type:
- Article
17
Erratum.
- Published in:
- Clinical Genetics, 2002, v. 61, n. 2, p. 167, doi. 10.1034/j.1399-0004.2002.610216.x
- Publication type:
- Article