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)


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)


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)


LETTER

Heterozygous TGFBR2 mutations in Marfan syndrome

Takeshi Mizuguchi et al.

Nature Genetics 36, 855 - 860 (4 July 2004)


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)