Isolation of single circulating trophoblasts from maternal circulation for noninvasive fetal copy number variant profiling-Reference-Cited by-同舟云学术

Isolation of single circulating trophoblasts from maternal circulation for noninvasive fetal copy number variant profiling

Published:2022-12-08 Issue:1 Volume:43 Page:14-27
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Doffini Anna¹,Forcato Claudio¹,Mangano Chiara¹,Lattuada Debora²,Aversa Roberta¹,Maranta Chiara¹,Giovannone Emilia D.¹,Buson Genny¹,Bolognesi Chiara¹,Maiocchi Rebecca¹,Dori Martina¹,Jamal Liyana¹^ORCID,Ahmad Raidah B.¹,Yeo George S. H.³,Yeo Tai Wai³,Saragozza Silvia⁴,Silipigni Rosamaria⁵,Serafini Marta⁶,Biondi Andrea⁶,Perego Sofia⁷,Vergani Patrizia⁷,Ferrazzi Enrico²,Ricciardi‐Castagnoli Paola¹,Musci Thomas J.¹,Grati Francesca Romana¹⁴^ORCID

Affiliation:

1. A. Menarini Biomarkers Singapore Pte Ltd, R&D department Singapore Singapore

2. Department of Woman Child and Neonate, Obstetrics Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico Milan Italy

3. Department of Maternal Fetal Medicine KK Women's and Children's Hospital Singapore Singapore

4. Research and Development, Cytogenetics and Molecular Genetics TOMA Advanced Biomedical Assays S.p.A., Impact Lab Busto Arsizio Italy

5. Laboratory of Medical Genetics, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico Milan Italy

6. Centro Ricerca M. Tettamanti, Department of Pediatrics University of Milano‐Bicocca Monza Italy

7. Department of Obstetrics and Gynecology MBBM Foundation Onlus at San Gerardo Hospital Monza Italy

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6275

Reference34 articles.

1. Current use of noninvasive prenatal testing in Europe, Australia and the USA: A graphical presentation

2. Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

3. Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound

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