Found: 11
Select item for more details and to access through your institution.
PCR-generated padlock probes distinguish homologous chromosomes through quantitative fluorescence analysis.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 357, doi. 10.1038/sj.ejhg.5200966
- By:
- Publication type:
- Article
Measured haplotype analysis of the aldosterone synthase gene and heart size.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 395, doi. 10.1038/sj.ejhg.5200967
- By:
- Publication type:
- Article
Spatial patterns of cystic fibrosis mutation spectra in European populations.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 385, doi. 10.1038/sj.ejhg.5200970
- By:
- Publication type:
- Article
Cys611Ser mutation in RET proto-oncogene in a kindred with medullary thyroid carcinoma and Hirschsprung's disease.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 364, doi. 10.1038/sj.ejhg.5200971
- By:
- Publication type:
- Article
Multiplex single-tube screening for mutations in the Nijmegen Breakage Syndrome (NBS1) gene in Hodgkin's and non-Hodgkin's lymphoma patients of Slavic origin.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 416, doi. 10.1038/sj.ejhg.5200972
- By:
- Publication type:
- Article
Transient expression of wild-type and mutant glucocerebrosidases in hybrid vaccinia expression system.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 369
- By:
- Publication type:
- Article
Influence of missense mutation and silent mutation of LHB-subunit gene in Japanese patients with ovulatory disorders.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 402, doi. 10.1038/sj.ejhg.5200968
- By:
- Publication type:
- Article
Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 375, doi. 10.1038/sj.ejhg.5200975
- By:
- Publication type:
- Article
Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 420, doi. 10.1038/sj.ejhg.5200981
- By:
- Publication type:
- Article
MUC1 polymorphism confers increased risk for intestinal metaplasia in a Colombian population with chronic gastritis.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 380, doi. 10.1038/sj.ejhg.5200978
- By:
- Publication type:
- Article
A new locus for postaxial polydactyly type A/B on chromosome 7q21-q34.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 409, doi. 10.1038/sj.ejhg.5200982
- By:
- Publication type:
- Article