Chumei Li Li
7PUBLICATIONS
32CO-AUTHORS
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Publications (7)
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|Dec 03, 2022
Further characterization of the 9q31 microdeletion phenotype; delineation of a common region of overlap containing ZNF462.Lauren Brady, Mark Ballantyne, John Duck
|Nov 10, 2022
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data.Taila Hartley, Élisabeth Soubry, Meryl Acker
|May 27, 2021
TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study.Bradley Bowles, Alejandro Ferrer, Carla J Nishimura
|Feb 14, 2018
Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome.Yuri A Zarate, Constance L Smith-Hicks, Carol Greene
|Feb 01, 2017
Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.Y A Zarate, L Kalsner, A Basinger
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Frequent Collaborators
2 joint publications
Yuri A Zarate
2 joint publications
Mark Tarnopolsky
1 joint publications
Constance L Smith-Hicks
1 joint publications
Meena Balasubramanian
1 joint publications
Samantha Schrier Vergano
1 joint publications
David B Everman
1 joint publications
Bradley Bowles
1 joint publications
Alejandro Ferrer
1 joint publications
Jennifer Sullivan
1 joint publications
Emanuele Agolini
