Transcervical cells and the prenatal diagnosis of haemoglobin (Hb) mutations.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 358, doi. 10.1034/j.1399-0004.1999.560503.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1999 AND VI 56 AND IP 5
Results: 13
1
2
Cerebrotendinous xanthomatosis without xanthomas.
- Published in:
- 1999
- By:
- Publication type:
- Case Study
3
Hopes pinned on microarray technology to defeat TB.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 339, doi. 10.1034/j.1399-0004.1999.560501.1.x
- By:
- Publication type:
- Article
4
Genetics of sexual orientation.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 340, doi. 10.1034/j.1399-0004.1999.560501.2.x
- By:
- Publication type:
- Article
5
The malformed kidney: disruption of glomerular and tubular development.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 342, doi. 10.1034/j.1399-0004.1999.560502.x
- By:
- Publication type:
- Article
6
Antibody therapy for Alzheimer's disease.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 337, doi. 10.1034/j.1399-0004.1999.560501.x
- By:
- Publication type:
- Article
7
Mosaicism for a small marker chromosome resulting from a familial Robertsonian translocation (21;22).
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 363, doi. 10.1034/j.1399-0004.1999.560504.x
- By:
- Publication type:
- Article
8
Utility of the predictors of coronary heart disease mortality in a longitudinal study of elderly Finnish men aged 65 to 84 years is dependent on context defined by Apo E genotype and area of residence.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 368, doi. 10.1034/j.1399-0004.1999.560505.x
- By:
- Publication type:
- Article
9
Normolipidemia and hypercholesterolemia in persons heterozygous for the same 1592+5G→A splice site mutation in the low-density lipoprotein receptor gene.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 379, doi. 10.1034/j.1399-0004.1999.560506.x
- By:
- Publication type:
- Article
10
Genetic and segregation analysis of congenital cataract in the Indian population.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 389, doi. 10.1034/j.1399-0004.1999.560507.x
- By:
- Publication type:
- Article
11
Association between polymorphism of the cholecystokinin gene and idiopathic Parkinson's disease.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 395, doi. 10.1034/j.1399-0004.1999.560508.x
- By:
- Publication type:
- Article
12
Polyvariant mutant CFTR genes in patients with chronic pancreatitis.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 5, p. 401, doi. 10.1034/j.1399-0004.1999.560509.x
- By:
- Publication type:
- Article
13
Role of the Pro23Leu mutation in a family affected by retinitis pigmentosa in the Basque Country.
- Published in:
- 1999
- By:
- Publication type:
- Case Study