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Plos One|September 1, 2010
A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33Ryan N Traylor, Damien L Bruno, Trent Burgess, et al.American Journal of Medical Genetics. Part A|June 15, 2011
Phenotypic variability of distal 22q11.2 copy number abnormalitiesTiong Yang Tan, Amanda Collins, Paul A James, et al.Prenatal Diagnosis|November 22, 2012
Application of a new molecular technique for the genetic evaluation of products of conceptionFrancesca R Grati, Denise Molina Gomes, Devika Ganesamoorthy, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 16, 2019
Phase I Trial of Inducible Caspase 9 T Cells in Adult Stem Cell Transplant Demonstrates Massive Clonotypic Proliferative Potential and Long-term Persistence of Transgenic T CellsPing Zhang, Jyothy Raju, Md Ashik Ullah, et al.The Lancet. Child & Adolescent Health|March 21, 2024
Host gene expression signatures to identify infection type and organ dysfunction in children evaluated for sepsis: a multicentre cohort studyLuregn J Schlapbach, Devika Ganesamoorthy, Clare Wilson, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 28, 2013
Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literatureFrédérique Béna, Damien L Bruno, Mats Eriksson, et al.Journal of Medical Genetics|May 11, 2010
Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypesDamien L Bruno, Britt-Marie Anderlid, Anna Lindstrand, et al.Pageof 3