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Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)
63 auth.
F. Pinto e Vairo,
J. Kemppainen,
C. R. Vitek,
Denise Whalen,
Kayla J Kolbert,
Kaitlin Sikkink,
Sarah A. Kroc,
Teresa M. Kruisselbrink,
Gabrielle F. Shupe,
Alyssa K. Knudson,
Elizabeth M. Burke,
Elle C. Loftus,
Lorelei A Bandel,
C. Prochnow,
Lindsay A. Mulvihill,
...
Brittany C Thomas,
Dale M. Gable,
C. Graddy,
G. G. M. Garzon,
Idara U. Ekpoh,
E. Porquera,
F. Fervenza,
M. Hogan,
Mireille El Ters,
K. Warrington,
John M. Davis,
M. Koster,
Amir B. Orandi,
M. Basiaga,
A. Vella,
Seema Kumar,
A. Creo,
A. Lteif,
S. Pittock,
P. Tebben,
Ejigayehu G. Abate,
A. Joshi,
Elizabeth H. Ristagno,
M. Patnaik,
L. Schimmenti,
Radhika Dhamija,
Sonia Sabrowsky,
Klaas Wierenga,
M. Keddis,
N. Samadder,
R. Presutti,
S. Robinson,
Michael C. Stephens,
L. Roberts,
W. Faubion,
Sherilyn W. Driscoll,
L. Wong-Kisiel,
D. Selcen,
E. Flanagan,
V. Ramanan,
Lauren M. Jackson,
M. Mauermann,
V. Ortega,
Sarah A. Anderson,
Stacy L. Aoudia,
E. Klee,
Tammy M. McAllister,
K. Lazaridis
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2 |
2023 |
2
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