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)


BRIEF COMMUNICATION

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Gregor Kuhlenbäumer et al.

Nature Genetics 37, 1044 - 1046 (25 September 2005)


BRIEF COMMUNICATION

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

Orna Levran et al.

Nature Genetics 37, 931 - 933 (21 August 2005)


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)


ARTICLE

A common inversion under selection in Europeans

Hreinn Stefansson et al.

Nature Genetics 37, 129 - 137 (16 January 2005)


BRIEF COMMUNICATION

Mutations in RAI1 associated with Smith?Magenis syndrome

Rebecca E. Slager et al.

Nature Genetics 33, 466 - 468 (24 March 2003)