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Metabolism: Clinical and Experimental|November 6, 2020
Association of DLL1 with type 1 diabetes in patients characterized by low polygenic risk scoreJingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.
Experimental Biology and Medicine (Maywood, N.J.)|April 30, 2021
New insights into hallux valgus by whole exome sequencing studyJun Jia, Junyi Li, Huiqi Qu, et al.
European Journal of Human Genetics : EJHG|May 23, 2022
Genetics etiologies and genotype phenotype correlations in a cohort of individuals with central conducting lymphatic anomalyMandi Liu, Christopher L Smith, David M Biko, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 12, 2009
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumorsEric M Jackson, Angela J Sievert, Xiaowu Gai, et al.
Genome Biology|July 10, 2026
Computational strategies for copy number variation detection, disease association, and beyondAmir Hossein Saeidian, Hani Sabaie, Mahdi Akbarzadeh, et al.
Pediatric Diabetes|January 8, 2022
Improved genetic risk scoring algorithm for type 1 diabetes predictionHui-Qi Qu, Jingchun Qu, Joseph Glessner, et al.
The Journal of Pediatrics|May 19, 2009
Nocturnal enuresis: a suggestive endophenotype marker for a subgroup of inattentive attention-deficit/hyperactivity disorderJosephine Elia, Toshinobu Takeda, Rachel Deberardinis, et al.
Journal of the National Cancer Institute|March 18, 2014
Rare variants in TP53 and susceptibility to neuroblastomaSharon J Diskin, Mario Capasso, Maura Diamond, et al.
Frontiers in Genetics|April 10, 2023
Identification of copy number variants contributing to hallux valgusWentao Zhou, Jun Jia, Hui-Qi Qu, et al.
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