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Genetics and Molecular Research : GMR|May 13, 2015
Case Report: Whole-exome analysis of a child with polycystic kidney disease and ventriculomegalyM M Nabhan, H Abdelaziz, Y Xu, et al.
Clinical Genetics|June 23, 2015
Glanzmann thrombasthenia in Pakistan: molecular analysis and identification of novel mutationsA Haghighi, M Borhany, A Ghazi, et al.
The Journal of Physiology|November 3, 2001
The voltage-dependent Cl(-) channel ClC-5 and plasma membrane Cl(-) conductances of mouse renal collecting duct cells (mIMCD-3)J A Sayer, G S Stewart, S H Boese, et al.
BMC Developmental Biology|December 10, 2020
Expression patterns of ciliopathy genes ARL3 and CEP120 reveal roles in multisystem developmentL Powell, M Barroso-Gil, G J Clowry, et al.
Scientific Reports|October 15, 2021
A mutant wfs1 zebrafish model of Wolfram syndrome manifesting visual dysfunction and developmental delayG Cairns, F Burté, R Price, et al.
Plos One|January 29, 2020
Embryonic and foetal expression patterns of the ciliopathy gene CEP164L A Devlin, S A Ramsbottom, L M Overman, et al.
Clinical Nephrology|August 21, 2007
Rapid onset intratubular calcification following renal transplantation requiring urgent parathyroidectomyA Sewpaul, J A Sayer, M A S Mohamed, et al.
Kidney International|October 26, 2007
Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisisM T F Wolf, S Saunier, J F O'Toole, et al.
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