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American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndromeD A Pillers, W K Seltzer, B R Powell, et al.
Clinical Genetics|August 8, 2008
The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in NewfoundlandS J Moore, D J Buckley, A MacMillan, et al.
Microbiology Resource Announcements|July 17, 2026
Draft genome sequence of Cupriavidus necator DVZ60, an isolate from iodine-impacted Hanford groundwaterOluwatomiwa J Sunbare-Funto, Raissa K Kodia-Batamio, Jerome J O Oliver, et al.
Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.
Aging Cell|April 23, 2026
Senolytic Treatment With Fisetin Reverses Age-Related Endothelial Dysfunction Partially Mediated by SASP Factor CXCL12Sophia A Mahoney, Krystyna Mazan-Mamczarz, Dimitrios Tsitsipatis, et al.
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