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Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
The Journal of Pediatrics|July 24, 2007
Hemolytic uremic syndrome associated with invasive pneumococcal disease: the United kingdom experienceAoife M Waters, Larissa Kerecuk, David Luk, et al.
BMC Medical Education|November 29, 2019
Educational roles as a continuum of mentoring's role in medicine - a systematic review and thematic analysis of educational studies from 2000 to 2018Lalit Kumar Radha Krishna, Yaazhini Renganathan, Kuang Teck Tay, et al.
Nature Genetics|November 5, 1997
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type IIID B Simon, R S Bindra, T A Mansfield, et al.
British Journal of Cancer|November 20, 2002
Exposure to power frequency electric fields and the risk of childhood cancer in the UKJ Skinner, T J Mee, R P Blackwell, et al.
Journal of Medical Genetics|November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing lossE H Stover, K J Borthwick, C Bavalia, et al.
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