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Robert Wildin
Robert Wildin
St. Luke's Regional Medical Center
Subtelomere
Pediatrics
Spectrum disorder
Candidate gene
Intellectual disability
2
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19
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GATA2 in the lymphatic vasculature or MonoMAC syndrome and primary lymphedema reveal a key role for mutations in patients with MDS/AML GATA2 Loss-of-function germline
2012
Dennis D. Hickstein
Marshall S. Horwitz
Christopher N. Hahn
Hamish S. Scott
Natasha L. Harvey Babic
Peter Bardy
Akiko Shimamura
Michael Zhang
Tom D. Walsh
Steven M. Holland
Amy P. Hsu
Sarah Dyack
Conrad V. Fernandez
Chan-Eng Chong
Genevieve A. Secker
Yajuan J. Liu
Jill A. Rosenfeld
Robert Wildin
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A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33
2010
PLOS ONE
Ryan Traylor
Damien L. Bruno
Trent Burgess
Robert Wildin
Anne Spencer
Devika Ganesamoorthy
David J. Amor
Matthew Hunter
Michael S. Caplan
Jill A. Rosenfeld
Aaron Theisen
Beth S. Torchia
Lisa G. Shaffer
Blake C. Ballif
Howard R. Slater
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Citations (19)
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