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Clinical Chemistry|June 3, 1999
A two-year study of microscopic urinalysis competency using the urinalysis-review computer programM L Astion, S Kim, A Nelson, et al.Nature Genetics|May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated formY Trottier, D Devys, G Imbert, et al.Nature Genetics|February 1, 1995
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer proteinK Ouahchi, M Arita, H Kayden, et al.JID Innovations : Skin Science From Molecules to Population Health|October 28, 2025
Increased Risk of Postoperative Complications in Patients with Hypertension Undergoing Mohs Micrographic SurgeryAlexandra Elder, Henry Y Yang, Megan O'Donnell-Cappelli, et al.Human Molecular Genetics|February 1, 1994
The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane proteinJ Mosser, Y Lutz, M E Stoeckel, et al.Human Genetics|July 1, 1992
A 530kb YAC contig tightly linked to the Friedreich ataxia locus contains five CpG clusters and a new highly polymorphic microsatelliteR Fujita, G Sirugo, F Duclos, et al.American Journal of Human Genetics|January 1, 1991
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)F Rousseau, A Vincent, S Rivella, et al.American Journal of Human Genetics|July 1, 1995
Genetic linkage heterogeneity in myotubular myopathyF Samson, L Mesnard, M Heimburger, et al.Clinical Genetics|February 26, 2013
Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosisO M'hamdi, C Redin, C Stoetzel, et al.Journal of Cardiac Surgery|November 24, 2022
Routine endoscopic robotic cardiac tumor resection using an 8-mm working port and percutaneous cannulationJake L Rosen, Colin C Yost, Daniella H Wong, et al.Pageof 31