@ARTICLE{
author={Kohl Stefan,Hwang Daw-Yang,Dworschak Gabriel C,Hilger Alina C,Saisawat Pawaree,Vivante Asaf,Stajic Natasa,Bogdanovic Radovan M,Reutter Heiko M,Kehinde Elijah O,Tasic Velibor,Hildebrandt Friedhelm},
year={2014},
title={Mild Recessive Mutations in Six Fraser Syndrome-Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract},
journal={JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY},
volume={25},
number={9},
pages={1917-1922},
document_type={Article},
} 

@ARTICLE{
author={Hwang Daw-Yang,Dworschak Gabriel C,Kohl Stefan,Saisawat Pawaree,Vivante Asaf,Hilger Alina C,Reutter Heiko M,Soliman Neveen A,Bogdanovic Radovan M,Kehinde Elijah O,Tasic Velibor,Hildebrandt Friedhelm},
year={2014},
title={Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract},
journal={KIDNEY INTERNATIONAL},
volume={85},
number={6},
pages={1429-1433},
document_type={Article},
} 

@ARTICLE{
author={Hoskins Bethan E,Cramer Carl HII,Tasic Velibor,Kehinde Elijah O,Ashraf Shazia,Bogdanovic Radovan M,Hoefele Julia,Pohl Martin,Hildebrandt Friedhelm},
year={2008},
title={Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations},
journal={NEPHROLOGY DIALYSIS TRANSPLANTATION},
volume={23},
number={2},
pages={777-779},
document_type={Letter},
}