Short Report A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 400, doi. 10.1111/j.0009-9163.2004.0212.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2004 AND VI 65 AND IP 5
Results: 16
1
2
Short Report Mutations in the hMLH1 gene in Slovenian patients with gastric carcinoma.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 405, doi. 10.1111/j.0009-9163.2004.0234.x
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- Publication type:
- Article
3
Short Report Association between −250G/A polymorphism of the hepatic lipase gene promoter and coronary artery disease and HDL-C levels in a Southern Brazilian population.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 390, doi. 10.1111/j.0009-9163.2004.00243.x
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- Publication type:
- Article
4
Short Report Variations in high-density lipoprotein cholesterol in relation to physical activity and Taq 1B polymorphism of the cholesteryl ester transfer protein gene.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 412, doi. 10.1111/j.0009-9163.2004.0237.x
- By:
- Publication type:
- Article
5
Short Report Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 419, doi. 10.1111/j.0009-9163.2004.0238.x
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- Publication type:
- Article
6
Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 358, doi. 10.1111/j.1399-0004.2004.0239.x
- By:
- Publication type:
- Article
7
Images in Genetics Section Editor: Albert E. Chudley, e-mail: Genetic landmarks through philately – autism spectrum disorders: a genetic update.
- Published in:
- 2004
- By:
- Publication type:
- Other
8
Short Report Molecular heterogeneity in two families with auditory pigmentary syndromes: the role of neuroimaging and genetic analysis in deafness.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 384, doi. 10.1111/j.0009-9163.2004.00235.x
- By:
- Publication type:
- Article
9
Short Report Deletion of the TWIST gene in a large five-generation family.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 396, doi. 10.1111/j.0009-9163.2004.00244.x
- By:
- Publication type:
- Article
10
Letter to the Editor A novel microdeletion, del(2)(q22.3q23.3) in a mentally retarded patient, detected by array-based comparative genomic hybridization.
- Published in:
- 2004
- By:
- Publication type:
- Letter
11
HotSpot Getting at the heart of coronary disease.
- Published in:
- 2004
- By:
- Publication type:
- Other
12
HotSpot Genomics goes to the dogs.
- Published in:
- 2004
- By:
- Publication type:
- Other
13
Texas physicians' perceptions of genomic medicine as an innovation.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 368, doi. 10.1111/j.0009-9163.2004.00253.x
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- Publication type:
- Article
14
Short Report A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosis.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 378, doi. 10.1111/j.0009-9163.2004.00254.x
- By:
- Publication type:
- Article
15
Short Report Prenatal diagnosis of de novo X;autosome translocations.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 5, p. 423, doi. 10.1111/j.0009-9163.2004.00255.x
- By:
- Publication type:
- Article
16
Erratum.
- Published in:
- 2004
- Publication type:
- Correction Notice