Editor's choice

Genetics of dyslexia: the evolving landscape
Johannes Schumacher, Per Hoffmann, Christine Schmäl, Gerd Schulte-Körne, Markus M Nöthen

Journal of Medical Genetics May 2007, 44 (5) 289-297; DOI: 10.1136/jmg.2006.046516
X-linked retinoschisis: an update
Stephen K Sikkink, Susmito Biswas, Neil R A Parry, Paulo E Stanga, Dorothy Trump

Journal of Medical Genetics Apr 2007, 44 (4) 225-232; DOI: 10.1136/jmg.2006.047340
Challenges in the phenotypic characterisation of patients in genetic studies of coronary artery disease
Albert K Luo, Brian K Jefferson, Mario J Garcia, Geoffrey S Ginsburg, Eric J Topol

Journal of Medical Genetics Mar 2007, 44 (3) 161-165; DOI: 10.1136/jmg.2006.045732
Guidelines for the diagnosis and management of individuals with neurofibromatosis 1
Rosalie E Ferner, Susan M Huson, Nick Thomas, Celia Moss, Harry Willshaw, D Gareth Evans, Meena Upadhyaya, Richard Towers, Michael Gleeson, Christine Steiger, Amanda Kirby

Journal of Medical Genetics Feb 2007, 44 (2) 81-88; DOI: 10.1136/jmg.2006.045906
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2
Blanche P Alter, Philip S Rosenberg, Lawrence C Brody

Journal of Medical Genetics Jan 2007, 44 (1) 1-9; DOI: 10.1136/jmg.2006.043257

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