P804: Prenatal diagnosis of atypical Holt-Oram syndrome caused by a novel inherited intragenic TBX5 duplication: A rare mechanism with variable expressivity
Michael Mackley,
Rachel Silver,
Nicholas Watkins,
Elena Greenfeld,
Sarah Redmond,
Hui Jue Zhang,
Maian Roifman,
David Chitayat
Affiliations
Michael Mackley
Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON
Rachel Silver
The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, Toronto, ON
Nicholas Watkins
Division of Diagnostic Medical Genetics, Mount Sinai Hospital, Toronto, ON
Elena Greenfeld
Division of Diagnostic Medical Genetics, Mount Sinai Hospital, Toronto, ON
Sarah Redmond
Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON
Hui Jue Zhang
Maternal Fetal Medicine Clinic, Oak Valley Health, Markham, ON
Maian Roifman
The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, Toronto, ON
David Chitayat
The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, Toronto, ON
