Found: 14
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TP53haplotype-based analysis and incidence of post-angioplasty restenosis.
- Published in:
- 2004
- By:
- Publication type:
- Correction Notice
Two linked polymorphic mutations (A(TA)7TAA and T-3279G) ofUGT1A1as the principal cause of Gilbert syndrome.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 525, doi. 10.1007/s00439-004-1183-x
- By:
- Publication type:
- Article
The humanTlocus and spina bifida risk.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 475, doi. 10.1007/s00439-004-1185-8
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- Publication type:
- Article
FISH diagnosis of the common 57-kb deletion inCTNScausing cystinosis.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 510, doi. 10.1007/s00439-004-1170-2
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- Publication type:
- Article
Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 468, doi. 10.1007/s00439-004-1182-y
- By:
- Publication type:
- Article
Francis Galton: Pioneer of heredity and biometry (2003).
- Published in:
- 2004
- By:
- Publication type:
- Book Review
Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 459, doi. 10.1007/s00439-004-1174-y
- By:
- Publication type:
- Article
Mutational analysis ofOGG1,MYH,MTH1in FAP, HNPCC and sporadic colorectal cancer patients: R154HOGG1polymorphism is associated with sporadic colorectal cancer patients.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 498, doi. 10.1007/s00439-004-1186-7
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- Publication type:
- Article
Emery A.E.H., Muntoni F. (eds): Duchenne muscular dystrophy.
- Published in:
- 2004
- By:
- Publication type:
- Book Review
Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 515, doi. 10.1007/s00439-004-1187-6
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- Publication type:
- Article
Diet and the frequency of the alanine:glyoxylate aminotransferase Pro11Leu polymorphism in different human populations.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 504, doi. 10.1007/s00439-004-1191-x
- By:
- Publication type:
- Article
TheCLCAgene locus as a modulator of the gastrointestinal basic defect in cystic fibrosis.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 483, doi. 10.1007/s00439-004-1190-y
- By:
- Publication type:
- Article
Y chromosome haplogroups of elite Ethiopian endurance runners.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 492, doi. 10.1007/s00439-004-1202-y
- By:
- Publication type:
- Article
Mutations.
- Published in:
- Human Genetics, 2004, v. 115, n. 6, p. 531, doi. 10.1007/s00439-004-1197-4
- Publication type:
- Article