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The British Journal of Ophthalmology|January 25, 2005
Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 geneP K F Addison, V Berry, A C W Ionides, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|March 22, 2008
A comparison of pancreaticoduodenectomy with extended pancreaticoduodenectomy: a meta-analysis of 1909 patientsN Iqbal, R E Lovegrove, H S Tilney, et al.
Molecular Vision|April 26, 2006
A large deletion in the adRP gene PRPF31: evidence that haploinsufficiency is the cause of diseaseLeen Abu-Safieh, Eranga N Vithana, Irmela Mantel, et al.
European Journal of Human Genetics : EJHG|March 28, 2013
Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humansVanita Berry, Cheryl Gregory-Evans, Warren Emmett, et al.
Journal of Medical Genetics|June 4, 1998
A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19qM Papaioannou, D Bessant, A Payne, et al.
Human Reproduction (Oxford, England)|September 19, 2015
Effectiveness and safety as outcome measures in reproductive medicineM Braakhekke, E I Kamphuis, F Mol, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|April 22, 2019
Can patient-reported outcomes be used instead of clinician-reported outcomes and photographs as primary endpoints of late normal tissue effects in breast radiotherapy trials? Results from the IMPORT LOW trialIndrani S Bhattacharya, Joanne S Haviland, Penelope Hopwood, et al.
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