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Naslov Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association (Article)
Autori 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 
Info KIDNEY INTERNATIONAL, (2014), vol. 85 br. 6, str. 1310-1317
Projekat National Institutes of Health [R01-DK045345, R01-DK088767]; March of Dimes Foundation [6FY11-241]; Division of Intramural Research; National Human Genome Research Institute (NHGRI); National Institutes of Health and Human services; Bundesministerium fur B
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency (Article)
Autori Bogdanovic Radovan M Draaken Markus Toromanovic Alma Djordjevic Maja S Stajic Natasa Ludwig Michael 
Info PEDIATRIC NEPHROLOGY, (2010), vol. 25 br. 11, str. 2363-2368
Projekat Ministry of Science, Republic of Serbia [145046D]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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