The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome

Published:2016-07-25 Issue:1 Volume:37 Page:53-60
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Dugoff Lorraine¹,Mennuti Michael T.¹,McDonald-McGinn Donna M.²

Affiliation:

1. Department of OB/GYN, Divisions of Reproductive Genetics and Maternal Fetal Medicine; University of Pennsylvania; Philadelphia PA USA

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

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference77 articles.

1. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis;Driscoll;J Med Genet,1993

2. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11;Burn;J Med Genet,1993

3. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2;Matsuoka;Am J Med Genet,1994

4. Letter to the Editor: What's in a name? The 22q11.2 deletion;McDonald-McGinn;Am J Med Genet,1994

5. Autosomal dominant “Opitz” GBBB syndrome due to a 22q11.2 deletion;McDonald-McGinn;Am J Med Genet,1995

Cited by 27 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. High positive predictive value 22q11.2 microdeletion screening by prenatal cell‐free DNA testing that incorporates fetal fraction amplification;Prenatal Diagnosis;2024-04-15

2. Genetics of Common Birth Defects in Newborns;Principles of Neonatology;2024

3. Anomalías cardíacas fetales: diagnóstico prenatal y tratamiento perinatal;EMC - Ginecología-Obstetricia;2023-06

4. Noninvasive prenatal testing/screening by circulating cell-free DNA;Human Reproductive and Prenatal Genetics;2023

5. Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome;American Journal of Obstetrics and Gynecology;2022-07