Showing results (61-70 of 124) with videos related to

Sort By:
Pageof 13
Pediatrics|August 3, 2004
Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrumMelanie A Manning, Suzanne B Cassidy, Carol Clericuzio, et al.
Human Pathology|December 13, 2018
Immune checkpoint blockade as a potential therapeutic strategy for undifferentiated malignanciesKelly A Devereaux, Vivek Charu, Shuchun Zhao, et al.
The Journal of Craniofacial Surgery|January 26, 2013
RUNX2 quadruplication: additional evidence toward a new form of syndromic craniosynostosisMatthew R Greives, Eric A Odessey, Darrel J Waggoner, et al.
American Journal of Clinical Pathology|October 20, 2006
Evaluation of Her-2/neu status in carcinomas with amplified chromosome 17 centromere locusMegan L Troxell, Charles D Bangs, Helen J Lawce, et al.
Science (New York, N.Y.)|April 15, 2006
CTCF mediates interchromosomal colocalization between Igf2/H19 and Wsb1/Nf1Jian Qun Ling, Tao Li, Ji Fan Hu, et al.
Frontiers in Neurology|May 24, 2021
SMA Identified: Clinical and Molecular Findings From a Sponsored Testing Program for Spinal Muscular Atrophy in More Than 2,000 IndividualsB Monica Bowen, Rebecca Truty, Swaroop Aradhya, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 12, 2010
Characterization of D-cyclin proteins in hematolymphoid neoplasms: lack of specificity of cyclin-D2 and D3 expression in lymphoma subtypesRyan A Metcalf, Shuchun Zhao, Matthew W Anderson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG)Athena M Cherry, Yassmine M Akkari, Kimberly M Barr, et al.
Circulation. Genomic and Precision Medicine|February 19, 2025
Analysis of TTN Truncating Variants in >74 000 Cases Reveals New Clinically Relevant Gene RegionsMatteo Vatta, Ellen Regalado, Michael Parfenov, et al.
Neurology. Genetics|April 28, 2020
Clinical utility of multigene analysis in over 25,000 patients with neuromuscular disordersThomas L Winder, Christopher A Tan, Sarah Klemm, et al.
Pageof 13