Human Genome Collection

Chromosome 15

Archive

LETTER

Analysis of the DNA sequence and duplication history of human chromosome 15
Free access

Michael C. Zody et al.

Nature 440, 671-675 (30 March 2006)

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LETTER

Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)

Martin Zenker et al.

Nature Genetics 37, 1345 - 1350 (20 November 2005)

Abstract | Full Text | PDF | Supplementary Information

LETTER

A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

Shoji Seki et al.

Nature Genetics 37, 607 - 612 (1 May 2005)

Abstract | Full Text | PDF | Supplementary Information

LETTER

Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis?renal dysfunction?cholestasis (ARC) syndrome

Paul Gissen et al.

Nature Genetics 36, 400 - 404 (28 March 2004)

Abstract | Full Text | PDF | Supplementary Information

LETTER

Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

Elisabeth Verpy et al.

Nature Genetics 29, 345 - 349 (10 September 2001)

Abstract | Full Text | PDF | Supplementary Information