@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={Saisawat Pawaree,Kohl Stefan,Hilger Alina C,Hwang Daw-Yang,Gee Heon Yung,Dworschak Gabriel C,Tasic Velibor,Pennimpede Tracie,Natarajan Sivakumar,Sperry Ethan,Matassa Danilo S,Stajic Natasa,Bogdanovic Radovan M,De Blaauw Ivo,Marcelis Carlo LM,Wijers Charlotte HW,Bartels Enrika,Schmiedeke Eberhard,Schmidt Dominik,Maerzheuser Stefanie,Grasshoff-Derr Sabine,Holland-Cunz Stefan,Ludwig Michael,Noethen Markus M,Draaken Markus,Brosens Erwin,Heij Hugo,Tibboel Dick,Herrmann Bernhard G,Solomon Benjamin D,De Klein Annelies,van Rooij Iris ALM,Esposito Franca,Reutter Heiko M,Hildebrandt Friedhelm},
year={2014},
title={Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association},
journal={KIDNEY INTERNATIONAL},
volume={85},
number={6},
pages={1310-1317},
document_type={Article},
}