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Neuromuscular Disorders : NMD|August 1, 1996
X-linked myotubular myopathy: refinement of the critical gene regionZ Smolenicka, J Laporte, L Hu, et al.Neuromuscular Disorders : NMD|March 4, 1999
Characterization of 34 novel and six known MTM1 gene mutations in 47 unrelated X-linked myotubular myopathy patientsS M Tanner, V Schneider, N S Thomas, et al.Hormone Research|January 1, 1991
Short stature in a patient with cystic fibrosis caused by a 6.7-kb human growth hormone gene deletionP E Mullis, S Liechti-Gallati, L Di Silvio, et al.Human Genetics|October 28, 1997
Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCRS Kleinle, U Wiesmann, A Superti-Furga, et al.American Journal of Nephrology|January 1, 1995
Chronic metabolic alkalosis: not uncommon in young children with severe cystic fibrosisG Pedroli, S Liechti-Gallati, S Mauri, et al.The Journal of Clinical Endocrinology and Metabolism|May 20, 1998
A new polymorphic restriction site in the human 11 beta-hydroxysteroid dehydrogenase type 2 geneZ Smolenicka, E Bach, A Schaer, et al.Pediatric Research|October 1, 1991
Association between haplotypes and specific mutations in Swiss cystic fibrosis familiesS Liechti-Gallati, N Malik, M Alkan, et al.Neuromuscular Disorders : NMD|January 1, 1991
X-linked centronuclear myopathy: mapping the gene to Xq28S Liechti-Gallati, B Müller, T Grimm, et al.Lancet (London, England)|February 9, 1999
Association of two silent polymorphisms of platelet glycoprotein Ia/IIa receptor with risk of myocardial infarction: a case-control studyK Moshfegh, W A Wuillemin, M Redondo, et al.Human Genetics|March 1, 1989
Molecular deletion patterns in Duchenne and Becker type muscular dystrophyS Liechti-Gallati, M Koenig, L M Kunkel, et al.Pageof 6