Clinical genetics

Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13
Katrien Janssens, Ruth Gershoni-Baruch, Els Van Hul, Riva Brik, Nuria Guañabens, Nicola Migone, Leon A Verbruggen, Stuart H Ralston, Maryse Bonduelle, Lionel Van Maldergem, Filip Vanhoenacker, Wim Van Hul

Journal of Medical Genetics Apr 2000, 37 (4) 245-249; DOI: 10.1136/jmg.37.4.245
Detecting low penetrance genes in cancer: the way ahead
R S Houlston, I P M Tomlinson

Journal of Medical Genetics Mar 2000, 37 (3) 161-167; DOI: 10.1136/jmg.37.3.161
Shared decision making and non-directiveness in genetic counselling
Glyn Elwyn, Jonathon Gray, Angus Clarke

Journal of Medical Genetics Feb 2000, 37 (2) 135-138; DOI: 10.1136/jmg.37.2.135
Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32
Melissa M Lees, Robin M Winter, Sue Malcolm, Howard M Saal, Lyn Chitty

Journal of Medical Genetics Dec 1999, 36 (12) 888-892; DOI: 10.1136/jmg.36.12.888
X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27
Arnold L Christianson, Roger E Stevenson, C H van der Meyden, Julie Pelser, Francois W Theron, Petro L van Rensburg, Michael Chandler, Charles E Schwartz

Journal of Medical Genetics Oct 1999, 36 (10) 759-766; DOI: 10.1136/jmg.36.10.759
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
Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR
Rebeca Valero, Gemma Marfany, Rosario Gil-Benso, Maria de los Angeles Ibáñez, Isidora López-Pajares, Félix Prieto, Gaspar Rullan, Enric Sarret, Roser Gonzàlez-Duarte

Journal of Medical Genetics Sep 1999, 36 (9) 694-699; DOI: 10.1136/jmg.36.9.694
Autosomal recessive retinitis pigmentosa locusRP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family
Su-min Gu, Govindasamy Kumaramanickavel, C R Srikumari, Michael J Denton, Andreas Gal

Journal of Medical Genetics Sep 1999, 36 (9) 705-707; DOI: 10.1136/jmg.36.9.705
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus
Guy Van Camp, Henricus Kunst, Kris Flothmann, Wyman McGuirt, Jan Wauters, Henri Marres, Margriet Verstreken, Irina N Bespalova, Margit Burmeister, Paul H Van de Heyning, Richard J H Smith, Patrick J Willems, Cor W R J Cremers, Marci M Lesperance

Journal of Medical Genetics Jul 1999, 36 (7) 532-536; DOI: 10.1136/jmg.36.7.532
Clinical mitochondrial genetics
Patrick F Chinnery, Neil Howell, Richard M Andrews, Douglass M Turnbull

Journal of Medical Genetics Jun 1999, 36 (6) 425-436; DOI: 10.1136/jmg.36.6.425

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