Rena J Vanzo - JoVE Visualize

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Journal of Medical Genetics|January 10, 2016

Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndromeKaren S Ho, Sarah T South, Amanda Lortz, et al.

Scientific Reports|October 27, 2019

Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X TestingCharles H Hensel, Rena J Vanzo, Megan M Martin, et al.

Neurogenetics|February 8, 2013

MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathwaysAlex R Paciorkowski, Ryan N Traylor, Jill A Rosenfeld, et al.

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Showing results (11-20 of 13) with videos related to

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You have reached the last page of results.This site can display upto 13 results.

Journal of Medical Genetics|January 10, 2016

Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndromeKaren S Ho, Sarah T South, Amanda Lortz, et al.

Scientific Reports|October 27, 2019

Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X TestingCharles H Hensel, Rena J Vanzo, Megan M Martin, et al.

Neurogenetics|February 8, 2013

MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathwaysAlex R Paciorkowski, Ryan N Traylor, Jill A Rosenfeld, et al.

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