Heterogeneity of genetic alterationsin prostate cancer: evidence of the complex nature of the disease.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2313, doi. 10.1093/hmg/10.20.2313
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 2001 AND VI 10 AND IP 20
Results: 18
1
2
SCA1 molecular genetics: a historyof a 13 year collaboration against glutamines.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2307
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- Publication type:
- Article
3
Challenges in identifying geneticvariation affecting susceptibility to type 2 diabetes: examplesfrom studies of the calpain-10 gene.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2301
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- Publication type:
- Article
4
Exploring the molecular basisof Bardet–Biedl syndrome.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2293, doi. 10.1093/hmg/10.20.2293
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- Publication type:
- Article
5
Pharmacogenetics.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2261, doi. 10.1093/hmg/10.20.2261
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- Publication type:
- Article
6
Molecular genetics of age-relatedmacular degeneration.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2285, doi. 10.1093/hmg/10.20.2285
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- Publication type:
- Article
7
Fanconi anemia and DNA repair.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2253, doi. 10.1093/hmg/10.20.2253
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- Publication type:
- Article
8
Forty years of decoding the silencein X-chromosome inactivation.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2225
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- Publication type:
- Article
9
Nuclear genetic defects of oxidativephosphorylation.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2277
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- Publication type:
- Article
10
Inherited neurodegenerative diseases:the one-hit model of neurodegeneration.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2269, doi. 10.1093/hmg/10.20.2269
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- Publication type:
- Article
11
The birth and death of humansingle-nucleotide polymorphisms: new experimental evidence and implicationsfor human history and medicine.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2195, doi. 10.1093/hmg/10.20.2195
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- Publication type:
- Article
12
Human diseases with underlyingdefects in chromatin structure and modification.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2233, doi. 10.1093/hmg/10.20.2233
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- Publication type:
- Article
13
Sequence variation and diseasein the wake of the draft human genome.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2209, doi. 10.1093/hmg/10.20.2209
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- Publication type:
- Article
14
Triplex forming oligonucleotides:sequence-specific tools for gene targeting.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2243, doi. 10.1093/hmg/10.20.2243
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- Publication type:
- Article
15
Lessons from the human genome:transitions between euchromatin and heterochromatin.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2215, doi. 10.1093/hmg/10.20.2215
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- Publication type:
- Article
16
Population genomics: a bridgefrom evolutionary history to genetic medicine.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2199, doi. 10.1093/hmg/10.20.2199
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- Publication type:
- Article
17
Dynamic mutations: a decade ofunstable expanded repeats in human genetic disease.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2187, doi. 10.1093/hmg/10.20.2187
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- Publication type:
- Article
18
Recent advances in disordersof iron metabolism: mutations, mechanisms and modifiers.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2181, doi. 10.1093/hmg/10.20.2181
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- Publication type:
- Article