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Troy J Gliem

Showing results (1-10 of 10) with videos related to

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The Journal of Molecular Diagnostics : JMD|August 16, 2017
Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed, Paraffin-Embedded Products of Conception SpecimensTroy J Gliem, Umut Aypar
Human Pathology|September 8, 2022
Clinicopathological and genomic copy number variation analysis in nodular hidradenoma and hidradenocarcinoma with focus on prognostically important featuresHong Jiang, Kabeer Shah, Katelyn A Reed, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?Erik C Thorland, Patrick R Gonzales, Troy J Gliem, et al.
American Journal of Medical Genetics. Part A|September 4, 2010
Mucinous cystadenoma of ovary in a patient with juvenile polyposis due to 10q23 microdeletion: expansion of phenotypeNikola Babovic, Patricia S Simmons, Christopher Moir, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 20, 2023
Anaplastic Kaposi Sarcoma: A Clinicopathologic and Molecular Genetic AnalysisGrant M Fischer, Troy J Gliem, Patricia T Greipp, et al.
Journal of Pediatric Hematology/Oncology|January 4, 2021
Pediatric Myxopapillary Ependymomas: A Clinicopathologic EvaluationKathryn L Eschbacher, Amulya Nageswara Rao, Patricia T Greipp, et al.
Human Molecular Genetics|April 16, 2011
B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysisKatharina Hopp, Christina M Heyer, Cynthia J Hommerding, et al.
The Journal of Molecular Diagnostics : JMD|September 17, 2022
Single-Nucleotide Polymorphism Array for Histologically Ambiguous Melanocytic TumorsKatherine B Geiersbach, Troy J Gliem, Sarah M Jenkins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
The Journal of Molecular Diagnostics : JMD|August 16, 2017
Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed, Paraffin-Embedded Products of Conception SpecimensTroy J Gliem, Umut Aypar
Human Pathology|September 8, 2022
Clinicopathological and genomic copy number variation analysis in nodular hidradenoma and hidradenocarcinoma with focus on prognostically important featuresHong Jiang, Kabeer Shah, Katelyn A Reed, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?Erik C Thorland, Patrick R Gonzales, Troy J Gliem, et al.
American Journal of Medical Genetics. Part A|September 4, 2010
Mucinous cystadenoma of ovary in a patient with juvenile polyposis due to 10q23 microdeletion: expansion of phenotypeNikola Babovic, Patricia S Simmons, Christopher Moir, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 20, 2023
Anaplastic Kaposi Sarcoma: A Clinicopathologic and Molecular Genetic AnalysisGrant M Fischer, Troy J Gliem, Patricia T Greipp, et al.
Journal of Pediatric Hematology/Oncology|January 4, 2021
Pediatric Myxopapillary Ependymomas: A Clinicopathologic EvaluationKathryn L Eschbacher, Amulya Nageswara Rao, Patricia T Greipp, et al.
Human Molecular Genetics|April 16, 2011
B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysisKatharina Hopp, Christina M Heyer, Cynthia J Hommerding, et al.
The Journal of Molecular Diagnostics : JMD|September 17, 2022
Single-Nucleotide Polymorphism Array for Histologically Ambiguous Melanocytic TumorsKatherine B Geiersbach, Troy J Gliem, Sarah M Jenkins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Pageof 1