Found: 10
Select item for more details and to access through your institution.
Ancestral proportions and their association with skin pigmentation and bone mineral density in Puerto Rican women from New York city.
- Published in:
- Human Genetics, 2004, v. 115, n. 1, p. 57, doi. 10.1007/s00439-004-1125-7
- By:
- Publication type:
- Article
The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster.
- Published in:
- Human Genetics, 2004, v. 115, n. 1, p. 36, doi. 10.1007/s00439-004-1106-x
- By:
- Publication type:
- Article
SNTG1, the gene encoding γ1-syntrophin: a candidate gene for idiopathic scoliosis.
- Published in:
- Human Genetics, 2004, v. 115, n. 1, p. 81, doi. 10.1007/s00439-004-1121-y
- By:
- Publication type:
- Article
Eric Lander, David Page, Richard Lifton (eds): Annual review of genomics and human genetics (volume 4): Annual Reviews, Palo Alto, California, 2003 (ISBN 0-8243-3704-2) hardcover, $75.00.
- Published in:
- 2004
- By:
- Publication type:
- Book Review
Lipoprotein lipase gene is in linkage with blood pressure phenotypes in Chinese pedigrees.
- Published in:
- Human Genetics, 2004, v. 115, n. 1, p. 8, doi. 10.1007/s00439-004-1108-8
- By:
- Publication type:
- Article
Small marker chromosomes in two patients with segmental aneusomy for proximal 17p.
- Published in:
- Human Genetics, 2004, v. 115, n. 1, p. 1
- By:
- Publication type:
- Article
Mitochondrial DNA polymorphisms as risk factors for Parkinson’s disease and Parkinson’s disease dementia.
- Published in:
- Human Genetics, 2004, v. 115, n. 1, p. 29, doi. 10.1007/s00439-004-1123-9
- By:
- Publication type:
- Article
Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions.
- Published in:
- Human Genetics, 2004, v. 115, n. 1, p. 69, doi. 10.1007/s00439-004-1101-2
- By:
- Publication type:
- Article
The origin of the isolated population of the Faroe Islands investigated using Y chromosomal markers.
- Published in:
- Human Genetics, 2004, v. 115, n. 1, p. 19, doi. 10.1007/s00439-004-1117-7
- By:
- Publication type:
- Article
An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype.
- Published in:
- Human Genetics, 2004, v. 115, n. 1, p. 13, doi. 10.1007/s00439-004-1118-6
- By:
- Publication type:
- Article