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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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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