Clinical genetics

Gamma-S crystallin gene (CRYGS) mutation causes dominant progressive cortical cataract in humans
H Sun, Z Ma, Y Li, B Liu, Z Li, X Ding, Y Gao, W Ma, X Tang, X Li, Y Shen

Journal of Medical Genetics Sep 2005, 42 (9) 706-710; DOI: 10.1136/jmg.2004.028274
A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5
S G Cole, M E Begbie, G M F Wallace, C L Shovlin

Journal of Medical Genetics Jul 2005, 42 (7) 577-582; DOI: 10.1136/jmg.2004.028712
New approaches to investigating heterogeneity in complex traits
R Bomprezzi, P E Kovanen, R Martin

Journal of Medical Genetics Aug 2003, 40 (8) 553-559; DOI: 10.1136/jmg.40.8.553
Corneal dystrophy and perceptive deafness (Harboyan syndrome): CDPD1 maps to 20p13
M J Abramowicz, J Albuquerque-Silva, A Zanen

Journal of Medical Genetics Feb 2002, 39 (2) 110-112; DOI: 10.1136/jmg.39.2.110
Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36
Daniel J Hampshire, Emma Roberts, Yanick Crow, Jacquelyn Bond, Ammar Mubaidin, Abdul-Latif Wriekat, Amir Al-Din, C Geoffrey Woods

Journal of Medical Genetics Oct 2001, 38 (10) 680-682; DOI: 10.1136/jmg.38.10.680
A new gene (DYX3) for dyslexia is located on chromosome 2
Toril Fagerheim, Peter Raeymaekers, Finn Egil Tønnessen, Marit Pedersen, Lisbeth Tranebjærg, Herbert A Lubs

Journal of Medical Genetics Sep 1999, 36 (9) 664-669; DOI: 10.1136/jmg.36.9.664

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