Chromosome 18q-Syndrome and 1p terminal duplication in a patient with bilateral vesico-ureteral reflux: case report and literature revision
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Reference10 articles.
1. Treatment of Pediatric Vesicoureteral Reflux Using Endoscopic Injection of Hyaluronic Acid/Dextranomer Gel: Intermediate-term Experience by a Single Surgeon
2. A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity
3. Genetics of vesicoureteral reflux
4. A new deletion of 18q23 with few typical features of the 18q- syndrome.
5. The 18q deletion syndrome and analysis of the critical region for orofacial cleft at 18q22.3
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1. Case report of a novel phenotype in 18q deletion syndrome;Romanian Journal of Morphology and Embryology;2021-04-01
2. Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly;Pediatric Research;2017-05-24
3. 18q deletion is difficult to detect by prenatal diagnosis: a report of two cases and a discussion of the literature;Clinical and Experimental Obstetrics & Gynecology;2017-02-10
4. Case report of individual with cutaneous immunodeficiency and novel 1p36 duplication;The Application of Clinical Genetics;2016-01
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