Showing results (261-270 of 645) with videos related to

Sort By:
Pageof 65
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Enriching for Answers in Rare DiseasesYilei Fu, Adam C English, Luis F Paulin, et al.
Human Molecular Genetics|June 19, 2013
Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1)Melody Caramins, James G Colebatch, Matthew N Bainbridge, et al.
Gigascience|May 31, 2022
Construction of a new chromosome-scale, long-read reference genome assembly for the Syrian hamster, Mesocricetus auratusR Alan Harris, Muthuswamy Raveendran, Dustin T Lyfoung, et al.
Life Science Alliance|July 24, 2021
Sequencing of a central nervous system tumor demonstrates cancer transmission in an organ transplantMarie-Claude Gingras, Aniko Sabo, Maria Cardenas, et al.
Sexually Transmitted Diseases|October 29, 2019
Sexually Transmitted Infections in Pregnancy and Reproductive Health: Proceedings of the STAR Sexually Transmitted Infection Clinical Trial Group Programmatic MeetingAdriane Wynn, Claire C Bristow, Anthony D Cristillo, et al.
Sexually Transmitted Diseases|April 19, 2023
Characterization of Vaginal Microbial Community Dynamics in the Pathogenesis of Incident Bacterial Vaginosis, a Pilot StudyJacob H Elnaggar, John W Lammons, Christopher M Taylor, et al.
Genome Medicine|June 29, 2013
Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathyJames R Lupski, Claudia Gonzaga-Jauregui, Yaping Yang, et al.
Journal of Bacteriology|February 5, 2008
The complete genome sequence of Escherichia coli DH10B: insights into the biology of a laboratory workhorseTim Durfee, Richard Nelson, Schuyler Baldwin, et al.
Genome Research|December 6, 2008
A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genomeOliver A Hampton, Petra Den Hollander, Christopher A Miller, et al.
American Journal of Medical Genetics. Part A|August 5, 2015
Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndromeEnder Karaca, Ozge O Yuregir, Sevcan T Bozdogan, et al.
Pageof 65