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	1.	The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1. [electronic resource] by Materna-Kiryluk, Anna Kiryluk, Krzysztof Burgess, Katelyn E Bieleninik, Arkadiusz Sanna-Cherchi, Simone Gharavi, Ali G Latos-Bielenska, Anna Producer: 20140825 In: Pediatric nephrology (Berlin, Germany) vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome. [electronic resource] by Sanna-Cherchi, Simone Burgess, Katelyn E Nees, Shannon N Caridi, Gianluca Weng, Patricia L Dagnino, Monica Bodria, Monica Carrea, Alba Allegretta, Maddalena A Kim, Hyunjae R Perry, Brittany J Gigante, Maddalena Clark, Lorraine N Kisselev, Sergey Cusi, Daniele Gesualdo, Loreto Allegri, Landino Scolari, Francesco D'Agati, Vivette Shapiro, Lawrence S Pecoraro, Carmine Palomero, Teresa Ghiggeri, Gian M Gharavi, Ali G Producer: 20111207 In: Kidney international vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutations in DSTYK and dominant urinary tract malformations. [electronic resource] by Sanna-Cherchi, Simone Sampogna, Rosemary V Papeta, Natalia Burgess, Katelyn E Nees, Shannon N Perry, Brittany J Choi, Murim Bodria, Monica Liu, Yan Weng, Patricia L Lozanovski, Vladimir J Verbitsky, Miguel Lugani, Francesca Sterken, Roel Paragas, Neal Caridi, Gianluca Carrea, Alba Dagnino, Monica Materna-Kiryluk, Anna Santamaria, Giuseppe Murtas, Corrado Ristoska-Bojkovska, Nadica Izzi, Claudia Kacak, Nilgun Bianco, Beatrice Giberti, Stefania Gigante, Maddalena Piaggio, Giorgio Gesualdo, Loreto Vukic, Durdica Kosuljandic Vukojevic, Katarina Saraga-Babic, Mirna Saraga, Marijan Gucev, Zoran Allegri, Landino Latos-Bielenska, Anna Casu, Domenica State, Matthew Scolari, Francesco Ravazzolo, Roberto Kiryluk, Krzysztof Al-Awqati, Qais D'Agati, Vivette D Drummond, Iain A Tasic, Velibor Lifton, Richard P Ghiggeri, Gian Marco Gharavi, Ali G Producer: 20130829 In: The New England journal of medicine vol. 369 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Copy-number disorders are a common cause of congenital kidney malformations. [electronic resource] by Sanna-Cherchi, Simone Kiryluk, Krzysztof Burgess, Katelyn E Bodria, Monica Sampson, Matthew G Hadley, Dexter Nees, Shannon N Verbitsky, Miguel Perry, Brittany J Sterken, Roel Lozanovski, Vladimir J Materna-Kiryluk, Anna Barlassina, Cristina Kini, Akshata Corbani, Valentina Carrea, Alba Somenzi, Danio Murtas, Corrado Ristoska-Bojkovska, Nadica Izzi, Claudia Bianco, Beatrice Zaniew, Marcin Flogelova, Hana Weng, Patricia L Kacak, Nilgun Giberti, Stefania Gigante, Maddalena Arapovic, Adela Drnasin, Kristina Caridi, Gianluca Curioni, Simona Allegri, Franca Ammenti, Anita Ferretti, Stefania Goj, Vinicio Bernardo, Luca Jobanputra, Vaidehi Chung, Wendy K Lifton, Richard P Sanders, Stephan State, Matthew Clark, Lorraine N Saraga, Marijan Padmanabhan, Sandosh Dominiczak, Anna F Foroud, Tatiana Gesualdo, Loreto Gucev, Zoran Allegri, Landino Latos-Bielenska, Anna Cusi, Daniele Scolari, Francesco Tasic, Velibor Hakonarson, Hakon Ghiggeri, Gian Marco Gharavi, Ali G Producer: 20130214 In: American journal of human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)