Works matching IS 10184813 AND DT 2004 AND VI 12 AND IP 6
Results: 14
Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 489, doi. 10.1038/sj.ejhg.5201125
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- Article
Depletion of PKD1 by an antisense oligodeoxynucleotide induces premature G1/S-phase transition.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 433, doi. 10.1038/sj.ejhg.5201136
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- Article
Unbalanced segregation of a complex four-break 5q23-31 insertion in the 5p13 band in a malformed child.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 455, doi. 10.1038/sj.ejhg.5201150
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- Article
Admixture, migrations, and dispersals in Central Asia: evidence from maternal DNA lineages.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 495, doi. 10.1038/sj.ejhg.5201160
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- Article
Angiotensin I-converting enzyme polymorphisms, ACE level and blood pressure among Nigerians, Jamaicans and African-Americans.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 460, doi. 10.1038/sj.ejhg.5201166
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- Article
Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutations.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 441, doi. 10.1038/sj.ejhg.5201167
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Glycerol kinase deficiency: residual activity explained by reduced transcription and enzyme conformation.
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- 2004
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- Publication type:
- Directory
Tools for molecular risk-stratification for clinical purposes: CLL as a prototype.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 423, doi. 10.1038/sj.ejhg.5201220
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- Article
A comparison of different metaphase CGH methods for the detection of cryptic chromosome aberrations of defined size.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 447, doi. 10.1038/sj.ejhg.5201175
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- Article
Haplotype diversity and SNP frequency dependence in the description of genetic variation.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 469, doi. 10.1038/sj.ejhg.5201179
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Failure to detect DUP25 in lymphoblastoid cells derived from patients with panic disorder and control individuals representing European and American populations.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 505, doi. 10.1038/sj.ejhg.5201181
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- Article
Candidate gene approach in association studies: would the factor V Leiden mutation have been found by this approach?
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 478, doi. 10.1038/sj.ejhg.5201183
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- Article
A novel point mutation in the mitochondrial tRNA<sup>Trp</sup> gene produces a neurogastrointestinal syndrome.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 509, doi. 10.1038/sj.ejhg.5201185
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- Article
Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families.
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- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 483, doi. 10.1038/sj.ejhg.5201177
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- Article