Human Genome Collection
Human Genomics: Chromosome 17
Archive
LETTER
DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage
Free access
Donna M. Muzny et al.
Nature 440, 1045-1049 (20 April 2006)
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BRIEF COMMUNICATION
Mutations in SEPT9 cause hereditary neuralgic amyotrophy
Gregor Kuhlenbäumer et al.
Nature Genetics 37, 1044 - 1046 (25 September 2005)
Abstract | Full Text | PDF | Supplementary Information
BRIEF COMMUNICATION
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
Orna Levran et al.
Nature Genetics 37, 931 - 933 (21 August 2005)
Abstract | Full Text | PDF | Supplementary Information
BRIEF COMMUNICATION
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
Marieke Levitus et al.
Nature Genetics 37, 934 - 935 (21 August 2005)
Abstract | Full Text | PDF | Supplementary Information
ARTICLE
A common inversion under selection in Europeans
Hreinn Stefansson et al.
Nature Genetics 37, 129 - 137 (16 January 2005)
Abstract | Full Text | PDF | Supplementary Information
BRIEF COMMUNICATION
Mutations in RAI1 associated with Smith?Magenis syndrome
Rebecca E. Slager et al.
Nature Genetics 33, 466 - 468 (24 March 2003)
Abstract | Full Text | PDF | Supplementary Information
