Recommended practice for laboratory reporting of non-invasive prenatal testing of trisomies 13, 18 and 21: a consensus opinion-Reference-Cited by-同舟云学术

Recommended practice for laboratory reporting of non-invasive prenatal testing of trisomies 13, 18 and 21: a consensus opinion

Published:2017-06-08 Issue:7 Volume:37 Page:699-704
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Deans Zandra C.¹,Allen Stephanie²,Jenkins Lucy³,Khawaja Farrah¹,Hastings Ros J.⁴,Mann Kathy⁵,Patton Simon J.⁶,Sistermans Erik A.⁷^ORCID,Chitty Lyn S.⁸^ORCID

Affiliation:

1. UK NEQAS for Molecular Genetics, Department of Laboratory Medicine; Royal Infirmary of Edinburgh; Edinburgh UK

2. West Midlands Regional Genetics Laboratory; Birmingham Women's NHS Foundation Trust; Birmingham UK

3. North East Thames Regional Genetics Laboratory; Great Ormond Street Hospital; London UK

4. CEQAS, John Radcliffe Hospital; Oxford University Hospitals NHS Foundation Trust; Oxford UK

5. Genetics Department, Viapath Analytics; Guy's Hospital; London UK

6. EMQN, Manchester Centre for Genomic Medicine, St Mary's Hospital; Manchester University Hospitals NHS Foundation Trust; Manchester UK

7. Department of Clinical Genetics; VU University Medical Center Amsterdam; Amsterdam The Netherlands

8. UCL Great Ormond Street Institute of Child Health and Great Ormond Street NHS Foundation Trust; London UK

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

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4. Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast;Alberry;Prenat Diagn,2007

5. Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases;Wang;Genet Med,2015

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3. International Guidelines for Implementation of NIPT/cffDNA Testing;Prenatal Diagnostic Testing for Genetic Disorders;2023

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