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Genomics|July 1, 1993
Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosomeS Lindsay, A R Curtis, P Roustan, et al.Journal of the Indian Medical Association|June 1, 2004
Diagnostic evaluation of extrapulmonary tuberculosis by fine needle aspiraton (FNA) supplemented with AFB smear and cultureS K Sinha, M Chatterjee, S Bhattacharya, et al.Scientific Reports|January 20, 2016
Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosaAnna M Rose, Amna Z Shah, Giulia Venturini, et al.Ophthalmic Paediatrics and Genetics|December 1, 1986
A genetic linkage study of choroideremiaM Jay, A F Wright, J F Clayton, et al.Physiological Genomics|August 5, 2010
Mouse embryonic phenotyping by morphometric analysis of MR imagesM Zamyadi, L Baghdadi, J P Lerch, et al.The European Physical Journal. E, Soft Matter|May 20, 2010
Buckling-driven morphological transformation of droplets of a mixed colloidal suspension during evaporation-induced self-assembly by spray dryingD Sen, J S Melo, J Bahadur, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 14, 1998
Prognostic significance of peripheral blood and bone marrow tyrosinase messenger RNA in malignant melanomaR A Ghossein, D Coit, M Brennan, et al.Development (Cambridge, England)|August 1, 1991
The Msh-like homeobox genes define domains in the developing vertebrate eyeA P Monaghan, D R Davidson, C Sime, et al.Human Heredity|March 17, 1999
Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patientsV Kucinskas, A M Payne, D Ambrasiene, et al.Novartis Foundation Symposium|January 31, 2004
Dominant cone and cone-rod dystrophies: functional analysis of mutations in retGC1 and GCAP1David M Hunt, Susan E Wilkie, Richard Newbold, et al.Pageof 144