Human Genome Collection
Chromosome 1
Archive
ARTICLE
The DNA sequence and biological annotation of human chromosome 1
Free access
S. G. Gregory et al.
Nature 441, 315-321 (18 May 2006)
Abstract | Full Text | PDF | Supplementary Information
LETTERS TO NATURE
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome
Maria Eriksson et al.
Nature 423, 293-29 (15 May 2003)
Abstract | Full Text | PDF | Supplementary Information
LETTER
A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility
David Reich et al.
Nature Genetics 37, 1113 - 1118 (25 September 2005)
Abstract | Full Text | PDF | Supplementary Information
LETTER
Human recombination hot spots hidden in regions of strong marker association
Alec J Jeffreys et al.
Nature Genetics 37, 601 - 606 (8 May 2005)
ARTICLE
A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities
Yuta Kochi et al.
Nature Genetics 37, 478 - 485 (17 April 2005)
Abstract | Full Text | PDF | Supplementary Information
BRIEF COMMUNICATION
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
Stephan Züchner et al.
Nature Genetics 36, 449 - 451 (4 April 2004)
Abstract | Full Text | PDF | Supplementary Information
