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Volume 10, Issue 20, 1 October 2001
Review
Recent advances in disorders of iron metabolism: mutations, mechanisms and modifiers
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2181–2186, https://doi.org/10.1093/hmg/10.20.2181
Dynamic mutations: a decade of unstable expanded repeats in human genetic disease
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2187–2194, https://doi.org/10.1093/hmg/10.20.2187
The birth and death of human single-nucleotide polymorphisms: new experimental evidence and implications for human history and medicine
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2195–2198, https://doi.org/10.1093/hmg/10.20.2195
Article
Population genomics: a bridge from evolutionary history to genetic medicine
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2199–2207, https://doi.org/10.1093/hmg/10.20.2199
Review
Sequence variation and disease in the wake of the draft human genome
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2209–2214, https://doi.org/10.1093/hmg/10.20.2209
Lessons from the human genome: transitions between euchromatin and heterochromatin
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2215–2223, https://doi.org/10.1093/hmg/10.20.2215
Forty years of decoding the silence in X-chromosome inactivation
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2225–2232, https://doi.org/10.1093/hmg/10.20.2225
Human diseases with underlying defects in chromatin structure and modification
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2233–2242, https://doi.org/10.1093/hmg/10.20.2233
Triplex forming oligonucleotides: sequence-specific tools for gene targeting
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2243–2251, https://doi.org/10.1093/hmg/10.20.2243
Fanconi anemia and DNA repair
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2253–2259, https://doi.org/10.1093/hmg/10.20.2253
Pharmacogenetics
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2261–2267, https://doi.org/10.1093/hmg/10.20.2261
Inherited neurodegenerative diseases: the one-hit model of neurodegeneration
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2269–2275, https://doi.org/10.1093/hmg/10.20.2269
Nuclear genetic defects of oxidative phosphorylation
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2277–2284, https://doi.org/10.1093/hmg/10.20.2277
Molecular genetics of age-related macular degeneration
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2285–2292, https://doi.org/10.1093/hmg/10.20.2285
Exploring the molecular basis of Bardet–Biedl syndrome
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2293–2299, https://doi.org/10.1093/hmg/10.20.2293
Challenges in identifying genetic variation affecting susceptibility to type 2 diabetes: examples from studies of the calpain-10 gene
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2301–2305, https://doi.org/10.1093/hmg/10.20.2301
SCA1 molecular genetics: a history of a 13 year collaboration against glutamines
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2307–2311, https://doi.org/10.1093/hmg/10.20.2307
Heterogeneity of genetic alterations in prostate cancer: evidence of the complex nature of the disease
Human Molecular Genetics, Volume 10, Issue 20, 1 October 2001, Pages 2313–2318, https://doi.org/10.1093/hmg/10.20.2313
