Ethics

A Val227Ala polymorphism in the peroxisome proliferator activated receptor α (PPARα) gene is associated with variations in serum lipid levels
K Yamakawa-Kobayashi, H Ishiguro, T Arinami, R Miyazaki, H Hamaguchi

Journal of Medical Genetics Mar 2002, 39 (3) 189-191; DOI: 10.1136/jmg.39.3.189
ATM mutations in Finnish breast cancer patients
M Allinen, V Launonen, K Laake, L Jansen, P Huusko, H Kääriäinen, A-L Børresen-Dale, R Winqvist

Journal of Medical Genetics Mar 2002, 39 (3) 192-196; DOI: 10.1136/jmg.39.3.192
An aetiological study of 25 mentally retarded adults with autism
C D M van Karnebeek, I van Gelderen, G J Nijhof, N G Abeling, P Vreken, E J Redeker, A M van Eeghen, J M N Hoovers, R C M Hennekam

Journal of Medical Genetics Mar 2002, 39 (3) 205-213; DOI: 10.1136/jmg.39.3.205
Dilated cardiomyopathy, sudden cardiac death, hypoplastic discs, and retinal detachment: a new autosomal dominant syndrome
J A Goodship, J O'Sullivan, P F Chinnery, A K Ryan, N Ziakas, C M Hall, M Clarke

Journal of Medical Genetics Mar 2002, 39 (3) 221-223; DOI: 10.1136/jmg.39.3.221
Contribution of BRCA2 germline mutations to hereditary breast/ovarian cancer in Germany
U Hamann, X Liu, S Lange, H U Ulmer, A Benner, R J Scott

Journal of Medical Genetics Mar 2002, 39 (3) e12; DOI: 10.1136/jmg.39.3.e12
Human T and risk for neural tube defects
B Richter, A H Schultealbert, M C Koch

Journal of Medical Genetics Mar 2002, 39 (3) e14; DOI: 10.1136/jmg.39.3.e14
A genome wide scan for familial high myopia suggests a novel locus on chromosome 7q36
L Naiglin, C Gazagne, F Dallongeville, C Thalamas, A Idder, O Rascol, F Malecaze, P Calvas

Journal of Medical Genetics Feb 2002, 39 (2) 118-124; DOI: 10.1136/jmg.39.2.118
Partial trisomy 9p12p21.3 with a normal phenotype
M Stumm, J Müsebeck, H Tönnies, M Volleth, J Lemke, I Chudoba, P Wieacker

Journal of Medical Genetics Feb 2002, 39 (2) 141-144; DOI: 10.1136/jmg.39.2.141
Molecular changes in skin predict predisposition to breast cancer
V J James, B E Willis

Journal of Medical Genetics Feb 2002, 39 (2) e1; DOI: 10.1136/jmg.39.2.e1
Refined mapping of the gene for otopalatodigital syndrome type I
T Kosho, T Uemura, M Tanimura, H Ohashi, K Muroya, T Ogata

Journal of Medical Genetics Feb 2002, 39 (2) e7; DOI: 10.1136/jmg.39.2.e7

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