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American Journal of Human Genetics|October 30, 1998
X chromosome inactivation in carriers of Barth syndromeK H Orstavik, R E Orstavik, A K Naumova, et al.Mycoses|September 26, 2024
Understanding Global Access to Topical Onychomycosis Therapy: A Systematic Review and Meta-AnalysisS M Nasereddin, J L Li, O S Malallah, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1986
Brain gangliosides in the presenile dementia of PickP E Kamp, W A den Hartog Jager, J Maathuis, et al.Biochimica Et Biophysica Acta|March 24, 1993
Differentiation and proliferation of respiration-deficient human myoblastsN H Herzberg, R Zwart, R A Wolterman, et al.Nature Genetics|September 1, 1996
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contracturesG J Jöbsis, H Keizers, J P Vreijling, et al.Human Molecular Genetics|May 18, 2000
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)A Muchir, G Bonne, A J van der Kooi, et al.Annals of Neurology|October 1, 1996
Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathiesP H Meijerink, J E Hoogendijk, A A Gabreëls-Festen, et al.Journal of Inherited Metabolic Disease|February 4, 2012
Improving test properties for neonatal cystic fibrosis screening in the Netherlands before the nationwide start by May 1st 2011Martina C Cornel, Johan J P Gille, J Gerard Loeber, et al.The Journal of Biological Chemistry|August 8, 1998
SecDF of Bacillus subtilis, a molecular Siamese twin required for the efficient secretion of proteinsA Bolhuis, C P Broekhuizen, A Sorokin, et al.American Journal of Human Genetics|April 1, 1996
Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystoniaD D De Vries, L N Went, G W Bruyn, et al.Pageof 14