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Spinal Cord|June 1, 2005
Limits of locomotor ability in subjects with a spinal cord injuryH J A van Hedel, B Wirth, V Dietz
International Journal of Dermatology|January 1, 1992
Porokeratosis of Mibelli following heart transplantI L Rothman, P B Wirth, M V Klaus
Der Urologe. Ausg. A|November 1, 1993
[Therapy of prostate abscess by employing pigtail drainage with transrectal ultrasound control]B Wirth, T Loch, K Weichert-Jacobsen, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|December 1, 1995
[Improvement of interstitial brachytherapy for localized prostate neoplasms with a new implantation technique]G Kovács, R Galalae, B Wirth, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophyH Scheffer, J M Cobben, G Matthijs, et al.
Clinical Genetics|June 4, 2009
Protracted course of juvenile ceroid lipofuscinosis associated with a novel CLN3 mutation (p.Y199X)A Sarpong, G Schottmann, K Rüther, et al.
American Journal of Medical Genetics|September 24, 1999
Recurrent NF1 gene mutation in a patient with oligosymptomatic neurofibromatosis type 1 (NF1)A Buske, A Gewies, R Lehmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 1999
A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophyC L Lorson, E Hahnen, E J Androphy, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 29, 1997
Ocular findings in patients with autosomal dominant retinitis pigmentosa and Cys110Phe, Arg135Gly, and Gln344stop mutations of rhodopsinS Kremmer, A Eckstein, A Gal, et al.
The British Journal of Ophthalmology|August 1, 1993
Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsinE Apfelstedt-Sylla, M Kunisch, M Horn, et al.
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