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Beneficial Microbes|November 21, 2024
Limosilactobacillus reuteri ameliorates maternal separation stress in newborn mice and alters subsequent adult behaviourZ M Saleh, B Okeugo, V R Venna, et al.Human Molecular Genetics|March 1, 1995
Linkage of posterior polymorphous corneal dystrophy to 20q11E Héon, W D Mathers, W L Alward, et al.Nature Genetics|January 1, 1994
Three autosomal dominant corneal dystrophies map to chromosome 5qE M Stone, W D Mathers, G O Rosenwasser, et al.Hypertension (Dallas, Tex. : 1979)|August 7, 2023
Is Height2.7 Appropriate for Indexation of Left Ventricular Mass in Healthy Adolescents? The Importance of Sex DifferencesHannah C M Taylor, Nishi Chaturvedi, George Davey Smith, et al.Molecular Immunology|March 23, 2010
Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisitedS A Johnson, J M Williams, S Hakobyan, et al.British Journal of Pharmacology|April 18, 2009
Inhibition of colonic motility and defecation by RS-127445 suggests an involvement of the 5-HT2B receptor in rodent large bowel physiologyA K Bassil, C M Taylor, V J N Bolton, et al.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.Pageof 22