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Genetics in Medicine Open
(Jan 2024)
P311: Use of a DNA methylation signature for the diagnosis of TET3-related Beck-Fahrner syndrome and expansion of its related phenotype
Alice Man,
Matteo Di Scipio,
Rebecca Hough,
Haley McConkey,
Eric Diehl,
Christian Marshall,
Bekim Sadikovic,
Resham Ejaz
Affiliations
Alice Man
Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON, Canada
Matteo Di Scipio
Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON, Canada
Rebecca Hough
Division of Genetics, Department of Pediatrics, McMaster Children’s Hospital, Hamilton, ON, Canada
Haley McConkey
Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON, Canada
Eric Diehl
Sunnybrook Health Sciences Center, Toronto, ON, Canada
Christian Marshall
Division of Genome Diagnostics, The Hospital for Sick Children, Toronto, ON, Canada
Bekim Sadikovic
Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON, Canada
Resham Ejaz
Division of Genetics, Department of Pediatrics, McMaster Children’s Hospital, Hamilton, ON, Canada
Journal volume & issue
Vol. 2
p. 101206
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