Prenatal diagnosis of 22q11.2 deletion syndrome in twin pregnancy: A case report
Author:
Affiliation:
1. Maternal and Fetal Unit; Istanbul Bakirkoy Women and Children Hospital; Istanbul Turkey
2. Mardin Women's and Children's Hospital; Mardin Turkey
3. İzmir Tepecik Research Hospital; İzmir Turkey
Publisher
Wiley
Subject
Radiology, Nuclear Medicine and imaging
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jcu.21992/fullpdf
Reference19 articles.
1. Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q112 deletion syndromes;Kobrynski;Lancet,2007
2. Clinical features of 78 adults with 22q11 deletion syndrome;Bassett;Am J Med Genet A,2005
3. Genetic analyses in two extended families with deletion 22q11 syndrome: importance of extracardiac manifestations;Shooner;J Pediatr,2005
4. Velopharyngeal incompetence and chromosome 22q11 deletion;Boorman;Lancet,2001
5. The phenotype of adults with the 22q11 deletion syndrome: a review;Cohen;Am J Med Genet,1999
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center;Archives of Gynecology and Obstetrics;2021-06-18
2. Are Complete Blood Count Indices Different in Twins with the Diagnosis of Intrahepatic Cholestasis of Pregnancy?;Journal of Clinical Obstetrics & Gynecology;2020
3. Postnatal Diagnosis of 22q11.2 Deletion Syndrome in Fetal Megalourethra;Journal of Ultrasound in Medicine;2015-02
4. Syndrome de Di George;Prise en charge des maladies rares en anesthésie et analgésie obstétricales;2015
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