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Molecular Genetics & Genomic Medicine|January 21, 2016
Hutterite-type cataract maps to chromosome 6p21.32-p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac deathPhilip M Boone, Bo Yuan, Shen Gu, et al.Journal of Chemical Information and Modeling|November 28, 2006
New global communication process in thermodynamics: impact on quality of published experimental dataM Frenkel, R D Chirico, V Diky, et al.The Journal of Molecular Diagnostics : JMD|April 22, 2019
Leveraging Human Microbiome Features to Diagnose and Stratify Children with Irritable Bowel SyndromeEmily B Hollister, Numan Oezguen, Bruno P Chumpitazi, et al.Pediatric Blood & Cancer|June 17, 2022
Clinical and molecular features of pediatric cancer patients with Lynch syndromeSarah Scollon, Mohammad K Eldomery, Jacquelyn Reuther, et al.Plos One|March 26, 2015
Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regionsFuli Yu, Jian Lu, Xiaoming Liu, et al.Nucleic Acids Research|December 28, 2023
HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing dataHaowei Du, Zain Dardas, Angad Jolly, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 1, 2014
BCOR-CCNB3 fusions are frequent in undifferentiated sarcomas of male childrenTricia L Peters, Vijetha Kumar, Sumanth Polikepahad, et al.The Journal of Allergy and Clinical Immunology|January 14, 2018
Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatmentRaquel Ruiz-García, Alexander Vargas-Hernández, Ivan K Chinn, et al.Biorxiv : the Preprint Server for Biology|June 12, 2025
The SHR/Akr Y chromosome reveals repeated turnover of the rat pseudoautosomal regionDaniel W Bellott, Helen Skaletsky, Jennifer F Hughes, et al.Proceedings of the National Academy of Sciences of the United States of America|July 23, 2014
Next-generation sequencing identifies rare variants associated with Noonan syndromePeng-Chieh Chen, Jiani Yin, Hui-Wen Yu, et al.Pageof 65