Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome

Published:2018-07-28 Issue:8 Volume:176 Page:1735-1741
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet Part A

Author:

Schindewolf Erica¹^ORCID,Khalek Nahla¹,Johnson Mark P.¹,Gebb Juliana¹,Coleman Beverly¹,Crowley Terrence Blaine²,Zackai Elaine H.²,McDonald-McGinn Donna M.²,Moldenhauer Julie S.¹

Affiliation:

1. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia; Philadelphia Pennsylvania

2. Division of Human Genetics, Department of Pediatrics, 22q and You Center and Clinical Genetics Center, Children's Hospital of Philadelphia; the Perelman School of Medicine at the University of Pennsylvania; Philadelphia Pennsylvania

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.38665/fullpdf

Reference20 articles.

1. Practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;The Journal of Pediatrics,2011

2. A French collaborative survey of 272 fetuses with 22q11.2 deletion: Ultrasound findings, fetal autopsies and pregnancy outcomes;Besseau-Ayasse;Prenatal Diagnosis,2014

3. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: A 6-year prospective study;Boudjemline;Journal of Pediatrics,2001

4. Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome;Bretelle;European Journal of Medical Genetics,2010

5. The thymic-thoracic ratio in fetal heart defects: A simple way to identify fetuses at high risk for microdeletion 22q11;Chaoui;Ultrasound in Obstetrics and Gynecology,2011

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