Examination of Y-Chromosomal Microdeletions and Partial Microdeletions in Idiopathic Infertility in East Hungarian Patients

por Mokánszki, Attila, Ujfalusi, Anikó, Gombos, Éva, Balogh, István
Publicado 2018

Congenital Hyperinsulinism Caused by a De Novo Mutation in the ABCC8 Gene - A Case Report

por Molnár, Zsuzsanna, Balogh, Lfdia, Kappelmayer, János, Madar, László, Gombos, Éva, Balogh, István
Publicado 2017

Molecular Analysis of Cystic Fibrosis Patients in Hungary – An Update to the Mutational Spectrum

por Ivády, Gergely, Koczok, Katalin, Madar, Laszlo, Gombos, Eva, Toth, Izabella, Gyori, Klaudia, Balogh, István
Publicado 2015

Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations

por Kidd, Kendrah, Vylet’al, Petr, Schaeffer, Céline, Olinger, Eric, Živná, Martina, Hodaňová, Kateřina, Robins, Victoria, Johnson, Emily, Taylor, Abbigail, Martin, Lauren, Izzi, Claudia, Jorge, Sofia C., Calado, Joaquim, Torres, Rosa J., Lhotta, Karl, Steubl, Dominik, Gale, Daniel P., Gast, Christine, Gombos, Eva, Ainsworth, Hannah C., Chen, Ying Maggie, Almeida, Jorge Reis, de Souza, Cintia Fernandes, Silveira, Catarina, Raposeiro, Rita, Weller, Nelson, Conlon, Peter J., Murray, Susan L., Benson, Katherine A., Cavalleri, Gianpiero L., Votruba, Miroslav, Vrbacká, Alena, Amoroso, Antonio, Gianchino, Daniela, Caridi, Gianluca, Ghiggeri, Gian Marco, Divers, Jasmin, Scolari, Francesco, Devuyst, Olivier, Rampoldi, Luca, Kmoch, Stanislav, Bleyer, Anthony J.
Publicado 2020