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European Journal of Medical Genetics|March 5, 2013
Familial KANK1 deletion that does not follow expected imprinting patternRena J Vanzo, Megan M Martin, Mallory R Sdano, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Academia, advocacy, and industry: a collaborative method for clinical research advancementRena J Vanzo, Amanda Lortz, Amy R U L Calhoun, et al.
Molecular Genetics and Metabolism|June 26, 2012
Glutaric acidemia type 1: outcomes before and after expanded newborn screeningKrista Viau, Sharon L Ernst, Rena J Vanzo, et al.
American Journal of Medical Genetics. Part A|October 6, 2015
Mosaic deletion of 20pter due to rescue by somatic recombinationMegan M Martin, Rena J Vanzo, Mallory R Sdano, et al.
European Journal of Medical Genetics|May 6, 2018
Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disordersRena J Vanzo, Hope Twede, Karen S Ho, et al.
BMC Medical Genetics|March 21, 2018
Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysisAparna Prasad, Matthew A Sdano, Rena J Vanzo, et al.
Journal of Genetic Counseling|August 15, 2014
Clinical utility of chromosomal microarray analysis of DNA from buccal cells: detection of mosaicism in three patientsMallory R Sdano, Rena J Vanzo, Megan M Martin, et al.
Journal of Personalized Medicine|January 1, 2021
The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning AutismRena J Vanzo, Aparna Prasad, Lauren Staunch, et al.
Molecular Syndromology|July 11, 2017
A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson SyndromeAdrianne L Baxter, Jay L Vivian, R Tanner Hagelstrom, et al.
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