Showing results (821-830 of 872) with videos related to

Sort By:
Pageof 88
Molecular Phylogenetics and Evolution|June 18, 2010
Systematics of the subfamily Danioninae (Teleostei: Cypriniformes: Cyprinidae)Kevin L Tang, Mary K Agnew, M Vincent Hirt, et al.
Circulation|June 19, 1998
Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS RegistryE H Locati, W Zareba, A J Moss, et al.
The Pediatric Infectious Disease Journal|July 9, 1998
Prospective randomized double blind placebo-controlled evaluation of azithromycin for treatment of cat-scratch diseaseJ W Bass, B C Freitas, A D Freitas, et al.
Circulation|August 2, 2001
Clinical implications for affected parents and siblings of probands with long-QT syndromeJ Kimbrough, A J Moss, W Zareba, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|May 22, 2021
Prognostic factors associated with unhealed perineal wounds post-proctectomy for perianal Crohn's disease: a two-centre studyRebecca K Grant, Alfonso Elosua-González, Sonia Bouri, et al.
Clinical Genetics|April 19, 2003
KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden deathS Chen, L Zhang, R M Bryant, et al.
Arquivos De Neuro-Psiquiatria|February 25, 1999
[Prevalence and indirect costs of headache in a Brazilian Company]M Vincent, A de J Rodrigues, G V De Oliveira, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 18, 2019
Correction: Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy-number variantsTracy Brandt, Laura M Sack, Dolores Arjona, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2019
Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variantsTracy Brandt, Laura M Sack, Dolores Arjona, et al.
American Journal of Medical Genetics. Part A|June 24, 2025
An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical RecommendationsE Woods, N Holmes, A S Denommé-Pichon, et al.
Pageof 88