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Archives of Ophthalmology (Chicago, Ill. : 1960)|August 14, 2001
Real-time optical coherence tomography of the anterior segment at 1310 nmS Radhakrishnan, A M Rollins, J E Roth, et al.
The Journal of Clinical Investigation|December 26, 2001
A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)C Kranz, J Denecke, M A Lehrman, et al.
Journal of the American Chemical Society|April 9, 2020
Water-Compatible Cycloadditions of Oligonucleotide-Conjugated Strained Allenes for DNA-Encoded Library SynthesisMatthias V Westphal, Liam Hudson, Jeremy W Mason, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 22, 2020
Highly Selective, Amine-Derived Cannabinoid Receptor 2 ProbesMatthias V Westphal, Roman C Sarott, Elisabeth A Zirwes, et al.
The Journal of Clinical Investigation|April 29, 1998
Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapyR Niehues, M Hasilik, G Alton, et al.
The Journal of Pediatrics|June 4, 1999
Leukocyte adhesion deficiency II syndrome, a generalized defect in fucose metabolismT Marquardt, T Brune, K Lühn, et al.
Human Mutation|November 3, 2000
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)G Matthijs, E Schollen, C Bjursell, et al.
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