Human Genome Collection
Chromosome 3
Archive
LETTER
The DNA sequence, annotation and analysis of human chromosome 3
Free access
Donna M. Muzny et al.
Nature 440, 1194-1198 (27 April 2006)
Abstract | Full Text | PDF | Supplementary Information
BRIEF COMMUNICATION
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
Gaia Skibinski et al.
Nature Genetics 37, 806 - 808 (24 July 2005)
Abstract | Full Text | PDF | Supplementary Information
BRIEF COMMUNICATION
Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation
Inessa Grinberg et al.
Nature Genetics 36, 1053 - 1055 (29 August 2004)
Abstract | Full Text | PDF | Supplementary Information
LETTER
Heterozygous TGFBR2 mutations in Marfan syndrome
Takeshi Mizuguchi et al.
Nature Genetics 36, 855 - 860 (4 July 2004)
Abstract | Full Text | PDF | Supplementary Information
LETTER
A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome
Mark O'Driscoll et al.
Nature Genetics 33, 497 - 501 (17 March 2003)
BRIEF COMMUNICATION
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome
Jeanne Amiel et al.
Nature Genetics 33, 459 - 461 (17 March 2003)
Abstract | Full Text | PDF | Supplementary Information
