Array CGH analysis in high-risk pregnancies: comparing DNA from cultured cells and cell-free fetal DNA-Reference-Cited by-同舟云学术

Array CGH analysis in high-risk pregnancies: comparing DNA from cultured cells and cell-free fetal DNA

Published:2011-10-24 Issue:4 Volume:32 Page:383-388
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Gruchy Nicolas¹,Decamp Matthieu¹,Richard Nicolas²,Jeanne-Pasquier Corinne³,Benoist Guillaume⁴,Mittre Hervé²,Leporrier Nathalie¹

Affiliation:

1. Laboratoire de Cytogénétique Prénatale, Service de Génétique; CHU Caen Côte de Nacre, UFR de Médecine Caen; Caen France

2. Laboratoire de Génétique Moléculaire, Service de Génétique; CHU Caen Côte de Nacre, UFR de Médecine Caen; Caen France

3. Laboratoire d'Anatomie Pathologique; CHU Caen Côte de Nacre, UFR de Médecine Caen; Caen France

4. Service de Gynécologie Obstétrique et Médecine de la Reproduction; CHU Caen Côte de Nacre, UFR de Médecine Caen; Caen France

Funder

ABM

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.2861/fullpdf

Reference24 articles.

1. Large amounts of cell free fetal DNA are present in amniotic fluid;Bianchi;Clin Chem,2001

2. Prospective, interdisciplinary follow-up of children with prenatally diagnosed giant omphalocele: short term neurodevelopmental outcome;Danzer;J Pediatr Surg,2010

3. Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations;Evangelidou;Mol Cytogenet,2010

4. Chromosomal prenatal diagnosis: study of 936 cases of intrauterine abnormalities after ultrasound assessment;Eydoux;Prenat Diagn,1989

5. The karyotype of fetuses with anomalies detected by second trimester ultrasonography;Gonen;Eur J Obstet Gynecol Reprod Biol,1995

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