Glenda Hendson

Vancouver, BC, Canada

Last Updated: 09/26/2026

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Found 23 publications

Are CUL3 variants an underreported cause of congenital heart disease?

Are CUL3 variants an underreported cause of congenital heart disease?

Journal: American journal of medical genetics. Part A

Published: July 27, 2023

Lethal respiratory course and additional features expand the phenotypic spectrum of PIEZO2-related distal arthrogryposis type 5.

Lethal respiratory course and additional features expand the phenotypic spectrum of PIEZO2-related distal arthrogryposis type 5.

Journal: American journal of medical genetics. Part A

Published: January 06, 2022

Low-grade diffusely infiltrative tumour (LGDIT), SMARCB1-mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC.

Low-grade diffusely infiltrative tumour (LGDIT), SMARCB1-mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC.

Journal: Neuropathology and applied neurobiology

Published: August 31, 2021

Umbilical Cord Hemangioma with Significant Cord Edema.

Umbilical Cord Hemangioma with Significant Cord Edema.

Journal: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Published: June 22, 2021

An infant with congenital respiratory insufficiency and diaphragmatic paralysis: A novel BICD2 phenotype?

An infant with congenital respiratory insufficiency and diaphragmatic paralysis: A novel BICD2 phenotype?

Journal: American journal of medical genetics. Part A

Published: April 18, 2021

Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variants.

Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variants.

Journal: American journal of medical genetics. Part A

Published: February 16, 2021

Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex 1 deficiency.

Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex 1 deficiency.

Journal: Molecular genetics and metabolism reports

Published: April 04, 2019

Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency.

Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency.

Journal: Molecular genetics and metabolism reports

Published: July 06, 2018

Comparative RNA-Sequencing Analysis Benefits a Pediatric Patient With Relapsed Cancer.

Comparative RNA-Sequencing Analysis Benefits a Pediatric Patient With Relapsed Cancer.

Journal: JCO precision oncology

Published: January 01, 2018

Clinical, imaging, and immunohistochemical characteristics of focal cortical dysplasia Type II extratemporal epilepsies in children: analyses of an institutional case series.

Clinical, imaging, and immunohistochemical characteristics of focal cortical dysplasia Type II extratemporal epilepsies in children: analyses of an institutional case series.

Journal: Journal of neurosurgery. Pediatrics

Published: November 26, 2016

Compound heterozygous TRPV4 mutations in two siblings with a complex phenotype including severe intellectual disability and neuropathy.

Compound heterozygous TRPV4 mutations in two siblings with a complex phenotype including severe intellectual disability and neuropathy.

Journal: American journal of medical genetics. Part A

Published: November 01, 2016

Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?

Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?

Journal: Orphanet journal of rare diseases

Published: June 14, 2016

Showing 1-12 of 23

Last Updated: 09/26/2026