R. Stephens

Gene organisation, sequence variation and isochore structure at the centromeric boundary of the human MHC.

S Beck, S. Humphray, L. Rowen, 1999, Journal of molecular biology.

Isolation, sequencing and expression of RED, a novel human gene encoding an acidic-basic dipeptide repeat.

J. Trowsdale, P. Freemont, D. Charron, 1999, Gene.

A human TAPBP (TAPASIN)‐related gene, TAPBP‐R

J. Trowsdale, J. Lindquist, L. Pasquier, 2002, European journal of immunology.

Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene.

M. Pembrey, J. Mossman, S. Blunt, 1983, Archives of disease in childhood.

Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting.

G. Mirza, J. Ragoussis, Y. Kuroki, 1998, Journal of medical genetics.

A serpin gene cluster on human chromosome 6p25 contains PI6, PI9 and ELANH2 which have a common structure almost identical to the 18q21 ovalbumin serpin genes

G. Mirza, J. Ragoussis, P. Bird, 1998, Cytogenetic and Genome Research.