Works matching IS 03406717 AND DT 2003 AND VI 113 AND IP 6
Results: 14
DNA sequence variation of the human ABO-secretor locus (FUT2) in New Guinean populations: possible early human migration from Africa.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 534, doi. 10.1007/s00439-003-1013-6
- By:
- Publication type:
- Article
Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility loci.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 514, doi. 10.1007/s00439-003-1020-7
- By:
- Publication type:
- Article
Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 542, doi. 10.1007/s00439-003-1015-4
- By:
- Publication type:
- Article
Cytometric analysis of cell phenotype and function: D.A. McCarthy, M.G. Macey (eds), Cambridge University Press, ISBN 0-521-66029-7, £95.00, 140 US$, Hardcover, 413 pages, 2001.
- Published in:
- 2003
- By:
- Publication type:
- Book Review
Hypervariability of the membrane-associated mucin and cancer marker MUC1.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 473, doi. 10.1007/s00439-003-1011-8
- By:
- Publication type:
- Article
Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 522, doi. 10.1007/s00439-003-1006-5
- By:
- Publication type:
- Article
Y-chromosome lineages in Cabo Verde Islands witness the diverse geographic origin of its first male settlers.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 467, doi. 10.1007/s00439-003-1007-4
- By:
- Publication type:
- Article
NF1 exon 7 skipping and sequence alterations in exonic splice enhancers (ESEs) in a neurofibromatosis 1 patient.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 551, doi. 10.1007/s00439-003-1009-2
- By:
- Publication type:
- Article
Mutations.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 556, doi. 10.1007/s00439-003-1035-0
- Publication type:
- Article
Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 502, doi. 10.1007/s00439-003-0998-1
- By:
- Publication type:
- Article
Y-chromosome lineages in Cabo Verde Islands witness the diverse geographic origin of its first male settlers.
- Published in:
- 2003
- By:
- Publication type:
- Erratum
Members of the CDY family have different expression patterns: CDY1 transcripts have the best correlation with complete spermatogenesis.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 486, doi. 10.1007/s00439-003-0990-9
- By:
- Publication type:
- Article
De novo insertion of an Alu sequence in the coding region of the CLCN5 gene results in Dent's disease.
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 480, doi. 10.1007/s00439-003-0991-8
- By:
- Publication type:
- Article
Chromosomal phylogeny and evolution of gibbons (Hylobatidae).
- Published in:
- Human Genetics, 2003, v. 113, n. 6, p. 493, doi. 10.1007/s00439-003-0997-2
- By:
- Publication type:
- Article