Bernice Morrow

16PUBLICATIONS
95CO-AUTHORS
Developmental genetics (incl. sex determination)Gene mappingTissue engineeringHaematological tumoursCellular nervous system
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Publications (16)

|Mar 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Jhih-Rong Lin, Daniella Miller, Dana Luong

|Dec 08, 2025
Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 Deletions.

Tanner J Nelson, Daniel E McGinn, T Blaine Crowley

|May 02, 2024
Risk of meningomyelocele mediated by the common 22q11.2 deletion.

Keng Ioi Vong, Sangmoon Lee, Kit Sing Au

|Sep 13, 2023
Crk and Crkl Are Required in the Endocardial Lineage for Heart Valve Development.

Bingruo Wu, Brian Wu, Sonia Benkaci

|Jul 28, 2023
Crk/Crkl regulates early angiogenesis in mouse embryos by accelerating endothelial cell maturation.

Lijie Shi, Hansoo Song, Bin Zhou

|Jul 18, 2023
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS.

Yingjie Zhao, Yujue Wang, Lijie Shi

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