Repetitive Exon 45/46-Related Sequences of Human Ca<sup>2+</sup> Channel α<sub>1C</sub> Subunit Gene.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 241, doi. 10.1159/000022810
- By:
- Publication type:
- Article
Works matching IS 00015652 AND DT 1998 AND VI 48 AND IP 5
Results: 12
1
2
New DNA Polymorphisms Define Ethnically Distinct Haplotypes in the Human Transferrin Receptor Gene.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 245, doi. 10.1159/000022811
- By:
- Publication type:
- Article
3
Adult-Onset Primary Open Angle Glaucoma Does Not Localize to Chromosome 2cen-q13 in North American Families.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 251, doi. 10.1159/000022812
- By:
- Publication type:
- Article
4
DNA Analysis of the Fragile X Syndrome in an at Risk Pediatric Population in Croatia: Simple Clinical Preselection Criteria Can Considerably Improve the Cost-Effectiveness of Fragile X Screening Studies.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 256, doi. 10.1159/000022813
- By:
- Publication type:
- Article
5
Low-Order Polynomial Trends of Female-to-Male Map Distance Ratios along Human Chromosomes.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 266, doi. 10.1159/000022814
- By:
- Publication type:
- Article
6
No Evidence for an Association between a Variant of the Mast Cell Chymase Gene and Atopic Dermatitis Based on Case-Control and Haplotype-Relative-Risk Analyses.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 271, doi. 10.1159/000022815
- By:
- Publication type:
- Article
7
Multi-Locus Nonparametric Linkage Analysis of Complex Trait Loci with Neural Networks.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 275, doi. 10.1159/000022816
- By:
- Publication type:
- Article
8
A Novel in Frame Deletion of Codons 188-190 in the hMSH2 Gene of a Slovenian Patient with Hereditary Non-Polyposis Colorectal Cancer.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 285, doi. 10.1159/000022817
- By:
- Publication type:
- Article
9
Identification of a CA/TG Repeat Polymorphism Proximal to the Human DLX3 Gene.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 288, doi. 10.1159/000022818
- By:
- Publication type:
- Article
10
Detection of the apoB-3500 Mutation in a Russian Family with Coronary Heart Disease.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 291, doi. 10.1159/000022819
- By:
- Publication type:
- Article
11
Parental HLA Genes, Hormone Level and Offspring Sex Ratios: A Reply to James' Letter.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 293, doi. 10.1159/000022820
- By:
- Publication type:
- Article
12
<sup>160</sup>Thr Mutation in the Rhodopsin Gene Associated withRet initis pigmentosa.
- Published in:
- Human Heredity, 1998, v. 48, n. 5, p. 237, doi. 10.1159/000022809
- By:
- Publication type:
- Article