Literature DB >> 18654600

22q11.2 microdeletion syndrome is a common cause of renal tract malformations.

Stéphane Burtey.   

Abstract

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Year:  2008        PMID: 18654600     DOI: 10.1038/ncpneph0906

Source DB:  PubMed          Journal:  Nat Clin Pract Nephrol        ISSN: 1745-8323


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  3 in total

Review 1.  Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.

Authors:  Valentina P Capone; William Morello; Francesca Taroni; Giovanni Montini
Journal:  Int J Mol Sci       Date:  2017-04-11       Impact factor: 5.923

2.  Copy-number disorders are a common cause of congenital kidney malformations.

Authors:  Simone Sanna-Cherchi; Krzysztof Kiryluk; Katelyn E Burgess; Monica Bodria; Matthew G Sampson; Dexter Hadley; Shannon N Nees; Miguel Verbitsky; Brittany J Perry; Roel Sterken; Vladimir J Lozanovski; Anna Materna-Kiryluk; Cristina Barlassina; Akshata Kini; Valentina Corbani; Alba Carrea; Danio Somenzi; Corrado Murtas; Nadica Ristoska-Bojkovska; Claudia Izzi; Beatrice Bianco; Marcin Zaniew; Hana Flogelova; Patricia L Weng; Nilgun Kacak; Stefania Giberti; Maddalena Gigante; Adela Arapovic; Kristina Drnasin; Gianluca Caridi; Simona Curioni; Franca Allegri; Anita Ammenti; Stefania Ferretti; Vinicio Goj; Luca Bernardo; Vaidehi Jobanputra; Wendy K Chung; Richard P Lifton; Stephan Sanders; Matthew State; Lorraine N Clark; Marijan Saraga; Sandosh Padmanabhan; Anna F Dominiczak; Tatiana Foroud; Loreto Gesualdo; Zoran Gucev; Landino Allegri; Anna Latos-Bielenska; Daniele Cusi; Francesco Scolari; Velibor Tasic; Hakon Hakonarson; Gian Marco Ghiggeri; Ali G Gharavi
Journal:  Am J Hum Genet       Date:  2012-11-15       Impact factor: 11.025

3.  Prenatal screening of DiGeorge (22q11.2 deletion) syndrome by abnormalities of the great arteries among Thai pregnant women.

Authors:  Kuntharee Traisrisilp; Fuanglada Tongprasert; Kasemsri Srisupundit; Suchaya Luewan; Theera Tongsong
Journal:  Obstet Gynecol Sci       Date:  2020-04-14
  3 in total

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