E.A. Carlson (ed) Mendel’s Legacy: the origin of classical genetics (2004).
- Published in:
- 2004
- By:
- Publication type:
- Book Review
Works matching IS 03406717 AND DT 2004 AND VI 115 AND IP 4
Results: 11
1
2
CHX10mutations cause non-syndromic microphthalmia/anophthalmia in Arab and Jewish kindreds.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 302, doi. 10.1007/s00439-004-1154-2
- By:
- Publication type:
- Article
3
Association between evolutionary history of angiotensinogen haplotypes and plasma levels.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 310, doi. 10.1007/s00439-004-1141-7
- By:
- Publication type:
- Article
4
Variations in the C3, C3a receptor, and C5 genes affect susceptibility to bronchial asthma.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 295, doi. 10.1007/s00439-004-1157-z
- By:
- Publication type:
- Article
5
Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 327, doi. 10.1007/s00439-004-1163-1
- By:
- Publication type:
- Article
6
The origin and spread of theHFE-C282Y haemochromatosis mutation.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 269, doi. 10.1007/s00439-004-1152-4
- By:
- Publication type:
- Article
7
Genomic rearrangements at theIGHMBP2gene locus in two patients with SMARD1.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 319, doi. 10.1007/s00439-004-1156-0
- By:
- Publication type:
- Article
8
Inheritance mode of multiple sclerosis: the effect ofHLAclass II alleles is stronger than additive.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 280, doi. 10.1007/s00439-004-1169-8
- By:
- Publication type:
- Article
9
Gender- and age-specific contributions of additional DNA sequence variation in the 5' regulatory region of theAPOEgene to prediction of measures of lipid metabolism.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 331, doi. 10.1007/s00439-004-1165-z
- By:
- Publication type:
- Article
10
Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters,SLC23A1andSLC23A2.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 285, doi. 10.1007/s00439-004-1167-x
- By:
- Publication type:
- Article
11
Mutations.
- Published in:
- Human Genetics, 2004, v. 115, n. 4, p. 347, doi. 10.1007/s00439-004-1161-3
- Publication type:
- Article