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Genome Research|January 24, 1998
A first-generation whole genome-radiation hybrid map spanning the mouse genomeL C McCarthy, J Terrett, M E Davis, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|November 29, 1995
The role of SOX9 in autosomal sex reversal and campomelic dysplasiaA J Schafer, M A Dominguez-Steglich, S Guioli, et al.
Neurogenetics|May 18, 1999
HLA typing in the United Kingdom multiple sclerosis genome screenF Coraddu, S Sawcer, R Feakes, et al.
Investigative Ophthalmology & Visual Science|July 13, 2000
Isolation of a novel iris-specific and leucine-rich repeat protein (oculoglycan) using differential selectionJ S Friedman, R Ducharme, V Raymond, et al.
Annals of Human Genetics|July 1, 1981
Deficiency of malic enzyme: a possible marker for malignancy in lymphoid cellsS Povey, S Jeremiah, E Arthur, et al.
Nuklearmedizin. Nuclear Medicine|February 16, 2005
Radioiodine uptake and thyroid hormone levels on or off simultaneous carbimazole medication: a prospective paired comparisonM A Walter, M Christ-Crain, B Müller, et al.
American Journal of Human Genetics|September 1, 1995
Mutation of the PAX6 gene in patients with autosomal dominant keratitisF Mirzayans, W G Pearce, I M MacDonald, et al.
Genomics|February 13, 2001
Isolation of a ubiquitin-like (UBL5) gene from a screen identifying highly expressed and conserved iris genesJ S Friedman, B F Koop, V Raymond, et al.
The EMBO Journal|October 1, 1990
The physical organization of the human immunoglobulin heavy chain gene complexM A Walter, U Surti, M H Hofker, et al.
American Journal of Medical Genetics|February 27, 2001
Genetic study of SOX9 in a case of campomelic dysplasiaJ Giordano, H M Prior, J S Bamforth, et al.
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