Pneumonia (infectious disease)

Association of susceptibility to the development of pneumonia in the older Japanese population with haem oxygenase-1 gene promoter polymorphism
H Yasuda, S Okinaga, M Yamaya, T Ohrui, M Higuchi, M Shinkawa, S Itabashi, K Nakayama, M Asada, A Kikuchi, S Shibahara, H Sasaki

Journal of Medical Genetics Apr 2006, 43 (4) e17; DOI: 10.1136/jmg.2005.035824
Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome
M Plasilova, C Chattopadhyay, P Pal, N A Schaub, S A Buechner, Hj Mueller, P Miny, A Ghosh, K Heinimann

Journal of Medical Genetics Aug 2004, 41 (8) 609-614; DOI: 10.1136/jmg.2004.019661
Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome
F Tassone, R J Hagerman, D Garcia-Arocena, E W Khandjian, C M Greco, P J Hagerman

Journal of Medical Genetics Apr 2004, 41 (4) e43; DOI: 10.1136/jmg.2003.012518
Molecular characterisation of a 3.5 Mb interstitial 14q deletion in a child with several phenotypic anomalies
E Petek, B Plecko-Startinig, C Windpassinger, H Egger, K Wagner, P M Kroisel

Journal of Medical Genetics Apr 2003, 40 (4) e47; DOI: 10.1136/jmg.40.4.e47

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