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Molecular Cytogenetics|June 12, 2025
Incorporating automation in a cytogenetics laboratory: three practitioners' perspectives on benefits and limitationsCecelia Miller, Jennie Thurston, Ninette Cohen
Child Neurology Open|May 21, 2019
De Novo Interstitial Deletion of 9q in a Pediatric Patient With Global Developmental DelayDennis Keselman, Ram Singh, Ninette Cohen, et al.
BMC Medical Genomics|March 20, 2019
Familial inheritance of the 3q29 microdeletion syndrome: case report and reviewWahab A Khan, Ninette Cohen, Stuart A Scott, et al.
Cancer Genetics and Cytogenetics|May 14, 2003
Clonal expansion and not cell interconversion is the basis for the neuroblast and nonneuronal types of the SK-N-SH neuroblastoma cell lineNinette Cohen, David R Betts, Gideon Rechavi, et al.
American Journal of Medical Genetics. Part A|December 14, 2007
Multiple hemangiomas in a patient with a t(3q;4p) translocation: an infrequent association with Wolf-Hirschhorn syndromeSherly Pardo, Netta Blitman, Bokyung Han, et al.
Human Molecular Genetics|June 24, 2010
Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndromeStuart A Scott, Ninette Cohen, Tracy Brandt, et al.
The Journal of Molecular Diagnostics : JMD|March 20, 2017
Chromosomal Microarray Detection of Constitutional Copy Number Variation Using Saliva DNAJennifer Reiner, Lisa Karger, Ninette Cohen, et al.
European Journal of Medical Genetics|September 24, 2013
46,XY disorder of sex development and developmental delay associated with a novel 9q33.3 microdeletion encompassing NR5A1Tracy Brandt, Leah Blanchard, Khyati Desai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2010
Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridizationStuart A Scott, Ninette Cohen, Tracy Brandt, et al.
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