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Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1996
Clinicopathologic correlations in acute retinal necrosis caused by herpes simplex virus type 2F M Rahhal, L M Siegel, V Russak, et al.Radiology|April 5, 2003
Breast masses: removal of all US evidence during biopsy by using a handheld vacuum-assisted device--initial experienceDavid E March, Bret F Coughlin, Ruth B Barham, et al.Chemico-Biological Interactions|February 11, 2010
Protection by pyridostigmine bromide of marmoset hemi-diaphragm acetylcholinesterase activity after soman exposureJulian R Haigh, Michael Adler, James P Apland, et al.Biochemical and Biophysical Research Communications|October 12, 2000
Genomic organization and amplification of the human desmosomal cadherin genes DSC1 and DSC3, encoding desmocollin types 1 and 3N V Whittock, D M Hunt, L Rickman, et al.Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.Journal of Medical Genetics|October 4, 2005
Prenatal detection of unbalanced chromosomal rearrangements by array CGHL Rickman, H Fiegler, C Shaw-Smith, et al.Optics Express|January 29, 2025
Standoff ultra-compact micro-Raman (SUCR) sensor for lunar surface explorationM Nurul Abedin, Luther W Beegle, Jennifer E Edmunson, et al.Peerj|August 15, 2019
The effect of platelet lysate in culture of PDLSCs: an in vitro comparative studyDuaa A Abuarqoub, Nazneen Aslam, Raghda B Barham, et al.Radiology|June 1, 1987
Multispectral analysis of MR images of the breastJ K Gohagan, E L Spitznagel, W A Murphy, et al.Human Molecular Genetics|May 20, 1999
N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaL Rickman, D Simrak, H P Stevens, et al.Pageof 4