Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s13256-016-0855-1.pdf
Reference18 articles.
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2. Pober BR. Genetic aspects of human congenital diaphragmatic hernia. Clin Genet. 2008;74:1–15.
3. Terui K, Taguchi T, Goishi K, Hayakawa M, Tazuke Y, Yokoi A, et al. Prognostic factors of gastroesophageal reflux disease in congenital diaphragmatic hernia: a multicenter study. Pediatr Surg Int. 2014;30:1129–34.
4. Peetsold MG, Heij HA, Kneepkens CMF, Nagelkerke AF, Huisman J, Gemke RJBJ. The long-term follow-up of patients with a congenital diaphragmatic hernia: a broad spectrum of morbidity. Pediatr Surg Int. 2009;25:1–17.
5. Brady PD, Srisupundit K, Devriendt K, Fryns J, Deprest JA, Vermeesch JR. Recent developments in the genetic factors underlying congenital diaphragmatic hernia. Fetal Diagn Ther. 2011;29:25–39.
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1. De Novo Duplication of 11p15 Associated With Congenital Diaphragmatic Hernia;Frontiers in Pediatrics;2018-04-25
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