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	1.	Scimitar syndrome in a case with VACTERL association. [electronic resource] by Fritz, Christian J Reutter, Heiko M Herberg, Ulrike Producer: 20151117 In: Cardiology in the young vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Gender-associated differences in the psychosocial and developmental outcome in patients affected with the bladder exstrophy-epispadias complex. [electronic resource] by Lee, Celine Reutter, Heiko M Grässer, Melanie F Fisch, Margit Noeker, Meinolf Producer: 20060227 In: BJU international vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Circulating microRNAs are associated with Pulmonary Hypertension and Development of Chronic Lung Disease in Congenital Diaphragmatic Hernia. [electronic resource] by Herrera-Rivero, Marisol Zhang, Rong Heilmann-Heimbach, Stefanie Mueller, Andreas Bagci, Soyhan Dresbach, Till Schröder, Lukas Holdenrieder, Stefan Reutter, Heiko M Kipfmueller, Florian Producer: 20191028 In: Scientific reports vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract. [electronic resource] by Kohl, Stefan Hwang, Daw-Yang Dworschak, Gabriel C Hilger, Alina C Saisawat, Pawaree Vivante, Asaf Stajic, Natasa Bogdanovic, Radovan Reutter, Heiko M Kehinde, Elijah O Tasic, Velibor Hildebrandt, Friedhelm Producer: 20141121 In: Journal of the American Society of Nephrology : JASN vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract. [electronic resource] by Hwang, Daw-Yang Dworschak, Gabriel C Kohl, Stefan Saisawat, Pawaree Vivante, Asaf Hilger, Alina C Reutter, Heiko M Soliman, Neveen A Bogdanovic, Radovan Kehinde, Elijah O Tasic, Velibor Hildebrandt, Friedhelm Producer: 20150209 In: Kidney international vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract. [electronic resource] by Kohl, Stefan Chen, Jing Vivante, Asaf Hwang, Daw-Yang Shril, Shirlee Dworschak, Gabriel C Van Der Ven, Amelie Sanna-Cherchi, Simone Bauer, Stuart B Lee, Richard S Soliman, Neveen A Kehinde, Elijah O Reutter, Heiko M Tasic, Velibor Hildebrandt, Friedhelm Producer: 20170913 In: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestation. [electronic resource] by Bagci, Soyhan Brosens, Erwin Tibboel, Dick De Klein, Annelies Ijsselstijn, Hanneke Wijers, Charlotte H W Roeleveld, Nel de Blaauw, Ivo Broens, Paul M van Rooij, Iris A L M Hölscher, Alice Boemers, Thomas M Pauly, Marcus Münsterer, Oliver J Schmiedeke, Eberhard Schäfer, Mattias Ure, Benno E Lacher, Martin Choinitzki, Vera Schumacher, Johannes Zwink, Nadine Jenetzky, Ekkehart Katzer, David Arand, Joerg Bartmann, Peter Reutter, Heiko M Producer: 20170706 In: European journal of pediatrics vol. 175 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. [electronic resource] by Bartels, Enrika Schulz, Anna C Mora, Nicole W Pineda-Alvarez, Daniel E Wijers, Charlotte H W Marcelis, Carlo M Stressig, Rüdiger Ritgen, Jochen Schmiedeke, Eberhard Mattheisen, Manuel Draaken, Markus Hoffmann, Per Hilger, Alina C Dworschak, Gabriel C Baudisch, Friederike Ludwig, Michael Bagci, Soyhan Müller, Andreas Gembruch, Ulrich Geipel, Annegret Berg, Christoph Bartmann, Peter Nöthen, Markus M van Rooij, Iris A L M Solomon, Benjamin D Reutter, Heiko M Producer: 20130116 In: Clinical dysmorphology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents. [electronic resource] by Khetarpal, Sumeet A Schjoldager, Katrine T Christoffersen, Christina Raghavan, Avanthi Edmondson, Andrew C Reutter, Heiko M Ahmed, Bouhouche Ouazzani, Reda Peloso, Gina M Vitali, Cecilia Zhao, Wei Somasundara, Amritha Varshini Hanasoge Millar, John S Park, YoSon Fernando, Gayani Livanov, Valentin Choi, Seungbum Noé, Eric Patel, Pritesh Ho, Siew Peng Kirchgessner, Todd G Wandall, Hans H Hansen, Lars Bennett, Eric P Vakhrushev, Sergey Y Saleheen, Danish Kathiresan, Sekar Brown, Christopher D Abou Jamra, Rami LeGuern, Eric Clausen, Henrik Rader, Daniel J Producer: 20170626 In: Cell metabolism vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways. [electronic resource] by Sang, Liyun Miller, Julie J Corbit, Kevin C Giles, Rachel H Brauer, Matthew J Otto, Edgar A Baye, Lisa M Wen, Xiaohui Scales, Suzie J Kwong, Mandy Huntzicker, Erik G Sfakianos, Mindan K Sandoval, Wendy Bazan, J Fernando Kulkarni, Priya Garcia-Gonzalo, Francesc R Seol, Allen D O'Toole, John F Held, Susanne Reutter, Heiko M Lane, William S Rafiq, Muhammad Arshad Noor, Abdul Ansar, Muhammad Devi, Akella Radha Rama Sheffield, Val C Slusarski, Diane C Vincent, John B Doherty, Daniel A Hildebrandt, Friedhelm Reiter, Jeremy F Jackson, Peter K Producer: 20110722 In: Cell vol. 145 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association. [electronic resource] by Saisawat, Pawaree Kohl, Stefan Hilger, Alina C Hwang, Daw-Yang Yung Gee, Heon Dworschak, Gabriel C Tasic, Velibor Pennimpede, Tracie Natarajan, Sivakumar Sperry, Ethan Matassa, Danilo S Stajić, Nataša Bogdanovic, Radovan de Blaauw, Ivo Marcelis, Carlo L M Wijers, Charlotte H W Bartels, Enrika Schmiedeke, Eberhard Schmidt, Dominik Märzheuser, Stefanie Grasshoff-Derr, Sabine Holland-Cunz, Stefan Ludwig, Michael Nöthen, Markus M Draaken, Markus Brosens, Erwin Heij, Hugo Tibboel, Dick Herrmann, Bernhard G Solomon, Benjamin D de Klein, Annelies van Rooij, Iris A L M Esposito, Franca Reutter, Heiko M Hildebrandt, Friedhelm Producer: 20150209 In: Kidney international vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development. [electronic resource] by Vivante, Asaf Kleppa, Marc-Jens Schulz, Julian Kohl, Stefan Sharma, Amita Chen, Jing Shril, Shirlee Hwang, Daw-Yang Weiss, Anna-Carina Kaminski, Michael M Shukrun, Rachel Kemper, Markus J Lehnhardt, Anja Beetz, Rolf Sanna-Cherchi, Simone Verbitsky, Miguel Gharavi, Ali G Stuart, Helen M Feather, Sally A Goodship, Judith A Goodship, Timothy H J Woolf, Adrian S Westra, Sjirk J Doody, Daniel P Bauer, Stuart B Lee, Richard S Adam, Rosalyn M Lu, Weining Reutter, Heiko M Kehinde, Elijah O Mancini, Erika J Lifton, Richard P Tasic, Velibor Lienkamp, Soeren S Jüppner, Harald Kispert, Andreas Hildebrandt, Friedhelm Producer: 20151029 In: American journal of human genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. [electronic resource] by van der Ven, Amelie T Connaughton, Dervla M Ityel, Hadas Mann, Nina Nakayama, Makiko Chen, Jing Vivante, Asaf Hwang, Daw-Yang Schulz, Julian Braun, Daniela A Schmidt, Johanna Magdalena Schapiro, David Schneider, Ronen Warejko, Jillian K Daga, Ankana Majmundar, Amar J Tan, Weizhen Jobst-Schwan, Tilman Hermle, Tobias Widmeier, Eugen Ashraf, Shazia Amar, Ali Hoogstraaten, Charlotte A Hugo, Hannah Kitzler, Thomas M Kause, Franziska Kolvenbach, Caroline M Dai, Rufeng Spaneas, Leslie Amann, Kassaundra Stein, Deborah R Baum, Michelle A Somers, Michael J G Rodig, Nancy M Ferguson, Michael A Traum, Avram Z Daouk, Ghaleb H Bogdanović, Radovan Stajić, Natasa Soliman, Neveen A Kari, Jameela A El Desoky, Sherif Fathy, Hanan M Milosevic, Danko Al-Saffar, Muna Awad, Hazem S Eid, Loai A Selvin, Aravind Senguttuvan, Prabha Sanna-Cherchi, Simone Rehm, Heidi L MacArthur, Daniel G Lek, Monkol Laricchia, Kristen M Wilson, Michael W Mane, Shrikant M Lifton, Richard P Lee, Richard S Bauer, Stuart B Lu, Weining Reutter, Heiko M Tasic, Velibor Shril, Shirlee Hildebrandt, Friedhelm Producer: 20190910 In: Journal of the American Society of Nephrology : JASN vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)