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Anticancer Research|November 1, 1987
Morphometric study of myocardial changes during puromycin aminonucleoside induced nephropathy in ratsW J van der Vijgh, D Van Velzen, J S Van der Poort, et al.American Journal of Medical Genetics|July 9, 1999
CAG repeat contraction in the androgen receptor gene in three brothers with mental retardationR F Kooy, E Reyniers, K Storm, et al.Nature Genetics|June 1, 1993
The full mutation in the FMR-1 gene of male fragile X patients is absent in their spermE Reyniers, L Vits, K De Boulle, et al.Human Molecular Genetics|November 1, 1995
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15G van Camp, P Coucke, W Balemans, et al.The American Journal of Otology|September 19, 2000
Audiometric analysis of a Belgian family linked to the DFNA10 locusM Verstreken, F Declau, I Schatteman, et al.BMC Health Services Research|March 16, 2020
Pain-related fear in adolescents with chronic musculoskeletal pain: process evaluation of an interdisciplinary graded exposure programC Dekker, J C M van Haastregt, J A M C F Verbunt, et al.Genomics|April 1, 1997
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.Pageof 9