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1 research outputs found
Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene
Author
A Kong
A McKenna
+72Â more
A Vivante
A Vivante
Alyssa A. Riley
Angela Myers
Arundhati S. Kale
B Yuan
C Gonzaga-Jauregui
C Gonzaga-Jauregui
Carolyn D. Applegate
Christine Eng
D Challis
Daryl A. Scott
David R. Roth
Dolores J. Lamb
Donna M. Muzny
DY Hwang
E Karaca
E Sollis
Edmond T. Gonzales
Eileen D. Brewer
Ewa Elenberg
FF Hamdan
HM Kearney
J Knijnenburg
James R. Lupski
Jill A. Rosenfeld
Joann Bodurtha
John W. Belmont
JW Groothoff
K Retterer
K Wang
KE McTaggart
Lior Borovik
M Barua
M Verbitsky
Matthew N. Bainbridge
MF Wangler
Michael C. Braun
Milen Velinov
Mini Michael
Mir Reza Bekheirnia
N Krumm
N Nicolaou
Nasim Bekheirnia
Neil A. Hanchard
Nicolette K. Janzen
O Mansoor
P Saisawat
Poyyapakkam R. Srivaths
PR Rosias
Richard A. Gibbs
Richard Alan Lewis
S Richards
S Sanna-Cherchi
S Sanna-Cherchi
S Sanna-Cherchi
Sarah J. Swartz
Scott E. Wenderfer
Shalini N. Jhangiani
Shen Gu
SW Chang
TL Stockley
Tomek Gambin
W McLaren
W Shu
William J. Craigen
X Liu
Y Jiang
Y Yang
Y Yang
Yaping Yang
Zeynep Hande Coban Akdemir
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
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