Jean Jordan-Mcgowan

Ottawa, ON, Canada

Last Updated: 09/26/2026

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Found 22 publications

TAF15::ZNF384 Mixed Phenotype Acute Leukemia With Complex Karyotype: Case Report With B-ALL Induction, Blinatumomab Bridging to Allogeneic Transplant and Literature Review.

TAF15::ZNF384 Mixed Phenotype Acute Leukemia With Complex Karyotype: Case Report With B-ALL Induction, Blinatumomab Bridging to Allogeneic Transplant and Literature Review.

Journal: Clinical case reports

Published: August 01, 2025

Genome Mapping Nomenclature.

Genome Mapping Nomenclature.

Journal: Cytogenetic and genome research

Published: October 30, 2023

Addenda to ISCN 2020.

Addenda to ISCN 2020.

Journal: Cytogenetic and genome research

Published: July 10, 2023

Familial inheritance of 14q terminal deletion syndrome and review of the literature.

Familial inheritance of 14q terminal deletion syndrome and review of the literature.

Journal: European journal of medical genetics

Published: March 10, 2023

Porokeratotic eccrine ostial and dermal duct nevus associated with an 11 megabase 3p deletion.

Porokeratotic eccrine ostial and dermal duct nevus associated with an 11 megabase 3p deletion.

Journal: Pediatric dermatology

Published: July 22, 2021

Re: International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts, by T. Liehr.

Re: International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts, by T. Liehr.

Journal: Cytogenetic and genome research

Published: April 20, 2021

ALU transposition induces familial hypertrophic cardiomyopathy.

ALU transposition induces familial hypertrophic cardiomyopathy.

Journal: Molecular genetics & genomic medicine

Published: April 03, 2019

Atypical Hepatic Mesenchymal Hamartoma: Histologic Appearance, Immunophenotype, and Molecular Findings.

Atypical Hepatic Mesenchymal Hamartoma: Histologic Appearance, Immunophenotype, and Molecular Findings.

Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society

Published: December 01, 2018

Adopting High-Resolution Allele Frequencies Substantially Expedites Variant Interpretation in Genetic Diagnostic Laboratories.

Adopting High-Resolution Allele Frequencies Substantially Expedites Variant Interpretation in Genetic Diagnostic Laboratories.

Journal: The Journal of molecular diagnostics : JMD

Published: August 28, 2018

Genetic Diagnostic Testing for Inherited Cardiomyopathies: Considerations for Offering Multi-Gene Tests in a Health Care Setting.

Genetic Diagnostic Testing for Inherited Cardiomyopathies: Considerations for Offering Multi-Gene Tests in a Health Care Setting.

Journal: The Journal of molecular diagnostics : JMD

Published: April 25, 2018

Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratory.

Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratory.

Journal: Journal of medical genetics

Published: April 24, 2018

Correction to: Use of multicolor fluorescence in situ hybridization to detect deletions in clinical tissue sections.

Correction to: Use of multicolor fluorescence in situ hybridization to detect deletions in clinical tissue sections.

Journal: Laboratory investigation; a journal of technical methods and pathology

Published: March 10, 2018

Showing 1-12 of 22

Last Updated: 09/26/2026