Robert J Shprintzen
2PUBLICATIONS
38CO-AUTHORS
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Publications (2)
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|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
|May 27, 2025
An antisense oligonucleotide-based strategy to ameliorate cognitive dysfunction in the 22q11.2 Deletion Syndrome.Pratibha Thakur, Martin Lackinger, Anastasia Diamantopoulou
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Frequent Collaborators
2 joint publications
Bernice E Morrow
1 joint publications
Martin Lackinger
1 joint publications
Joseph A Gogos
1 joint publications
Jhih-Rong Lin
1 joint publications
Daniella Miller
1 joint publications
T Blaine Crowley
1 joint publications
Amirhossein Hajianpour
1 joint publications
Tiffany Busa
1 joint publications
Damian Heine-Suñer
1 joint publications
Kathleen Angkustsiri
