A clinical-pathogenetic approach on associated anomalies and chromosomal defects supports novel candidate critical regions and genes for gastroschisis
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery,Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/article/10.1007/s00383-018-4331-4/fulltext.html
Reference115 articles.
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2. Salinas-Torres VM, Salinas-Torres RA, Cerda-Flores RM, Martínez-de-Villarreal LE (2018) Prevalence, mortality, and spatial distribution of gastroschisis in Mexico. J Pediatr Adolesc Gynecol 31:232–237
3. Hunter AG, Stevenson RE (2008) Gastroschisis: clinical presentation and associations. Am J Med Genet C Semin Med Genet 148C:219–330
4. Akhtar J, Skarsgard ED, Canadian Pediatric Surgery Network (CAPSNet) (2012) Associated malformations and the “hidden mortality” of gastroschisis. J Pediatr Surg 47:911–916
5. Benjamin B, Wilson GN (2014) Anomalies associated with gastroschisis and omphalocele: analysis of 2825 cases from the Texas Birth Defects Registry. J Pediatr Surg 49:514–519
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1. Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis;Molecular Genetics & Genomic Medicine;2020-03-12
2. Database for Gene Variants and Metabolic Networks Implicated in Familial Gastroschisis;Data;2019-07-11
3. Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall;International Journal of Molecular Sciences;2019-05-09
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