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Frontiers in Endocrinology|July 22, 2022
Case Report: Reversible Hyperglycemia Following Rapamycin Treatment for Atypical Choroid Plexus Papilloma in an InfantJiale Liu, Minjie Luo, Siyuan Lv, et al.
Journal of Carcinogenesis|May 15, 2009
Identification of possible genetic alterations in the breast cancer cell line MCF-7 using high-density SNP genotyping microarrayHui-Yun Wang, Danielle Greenawalt, Xiangfeng Cui, et al.
Journal of Translational Medicine|August 3, 2020
Patient specific circulating tumor DNA fingerprints to monitor treatment response across multiple tumorsJiaping Li, Wei Jiang, Jinwang Wei, et al.
Plos One|April 23, 2009
Genetic structures of copy number variants revealed by genotyping single spermMinjie Luo, Xiangfeng Cui, David Fredman, et al.
Cold Spring Harbor Molecular Case Studies|June 20, 2020
A germline PALB2 pathogenic variant identified in a pediatric high-grade gliomaYiming Zhong, Jeffrey Schubert, Jinhua Wu, et al.
American Journal of Medical Genetics. Part A|January 10, 2024
Recurrent missense variant identified in two unrelated families with MPZL2-related hearing loss, expanding the variant spectrum associated with DFNB111Emma Lo, Justin Blair, Nobuko Yamamoto, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 3, 2025
Genetically Distinct Acute Megakaryoblastic Leukemia following Low Hypodiploid B-Lymphoblastic Leukemia linked by TP53 MutationJaryse C Harris, Jeffrey Schubert, Brian Lockhart, et al.
Genome Research|February 3, 2005
A genotyping system capable of simultaneously analyzing >1000 single nucleotide polymorphisms in a haploid genomeHui-Yun Wang, Minjie Luo, Irina V Tereshchenko, et al.
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