Emanuel syndrome and congenital diaphragmatic hernia: A systematic review
Author:
Publisher
Elsevier BV
Subject
General Medicine,Pediatrics, Perinatology and Child Health,Surgery
Reference10 articles.
1. Emanuel syndrome;Emanuel,2007
2. Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): clinical features of 63 individuals;Carter;Am J Med Genet Part A,2009
3. The llq;22q translocation: a European collaborative analysis of 43 cases;Fraccaro;Hum Genet,1980
4. The llq;22q translocation: a collaborative study of 20 new cases and analysis of 110 families;Iselius;Hum Genet,1983
5. Prenatal diagnosis of supernumerary chromosome derivative (22) due to maternal balanced translocation in association with diaphragmatic hernia: a case report;Kadir;Prenat Diagn,1997
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1. Emanuel syndrome due to unusual pattern;Egyptian Journal of Medical Human Genetics;2024-02-12
2. Prenatal cfDNA Screening for Emanuel Syndrome and Other Unbalanced Products of Conception in Carriers of the Recurrent Balanced Translocation t(11;22): One Laboratory’s Retrospective Experience;Genes;2023-10-10
3. Auricular fistula: a review of its clinical manifestations, genetics, and treatments;Journal of Molecular Medicine;2023-07-17
4. Prenatal diagnosis of Emanuel syndrome – case series and review of the literature;Journal of Obstetrics and Gynaecology;2022-09-01
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