Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Journal of Human Genetics|September 21, 2018
Maternally inherited 133kb deletion of 14q32 causing Kagami-Ogata syndromeHou-Sung Jung, Stephanie E Vallee, Mary Beth Dinulos, et al.
Preventive Veterinary Medicine|August 18, 2019
Emerging Leptospira strain poses public health risk for dairy farmers in New ZealandY Yupiana, E Vallee, P Wilson, et al.
Antimicrobial Agents and Chemotherapy|December 1, 1992
In vivo efficacy of a new fluoroquinolone, sparfloxacin, against penicillin-susceptible and -resistant and multiresistant strains of Streptococcus pneumoniae in a mouse model of pneumoniaE Azoulay-Dupuis, E Vallee, B Veber, et al.
New Zealand Veterinary Journal|November 9, 2025
Machine learning for predicting climate change impacts on Pseudopithomyces chartarum spore counts: a risk indicator of facial eczemaM Wada, O Sagarasaeranee, N Cogger, et al.
Journal of Clinical Microbiology|December 1, 1995
Diagnosis of tuberculosis by Amplicor Mycobacterium tuberculosis test: a multicenter studyE Carpentier, B Drouillard, M Dailloux, et al.
Antimicrobial Agents and Chemotherapy|April 1, 1993
Efficacy and ocular penetration of sparfloxacin in experimental streptococcal endophthalmitisI Cochereau-Massin, J Bauchet, S Marrakchi-Benjaafar, et al.
Clinical and Diagnostic Laboratory Immunology|January 10, 1998
Western blot analysis of antibody response to pneumococcal protein antigens in a murine model of pneumoniaH Mouneimne, M Juvin, J L Beretti, et al.
New Zealand Veterinary Journal|February 12, 2025
Investigating animals and environments in contact with leptospirosis patients in Aotearoa New Zealand reveals complex exposure pathwaysJ Benschop, J M Collins-Emerson, E Vallee, et al.
Frontiers in Pharmacology|October 20, 2025
Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disordersAmaël Davakan, Leos Cmarko, Barbara Ribeiro Oliveira-Mendes, et al.
American Journal of Human Genetics|May 3, 2016
A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT ComplexJing You, Nara L Sobreira, Dustin L Gable, et al.
Pageof 3