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Browsing by Author Dworschak, Gabriel C
Showing results 1 to 3 of 3
Issue Date | Title | Author(s) | Type | М-cat. |
---|---|---|---|---|
2014 | Mild Recessive Mutations in Six Fraser Syndrome-Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract | 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;
| Article | 21aM21a |
2014 | Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract | 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;
| Article | 21aM21a |
2014 | Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association | 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;
| Article | 21aM21a |