Noninvasive prenatal screening for cystic fibrosis using circulating trophoblasts: Detection of the 50 most common disease‐causing variants-Reference-Cited by-同舟云学术

Noninvasive prenatal screening for cystic fibrosis using circulating trophoblasts: Detection of the 50 most common disease‐causing variants

Published:2022-12-08 Issue:1 Volume:43 Page:3-13
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Jeppesen Line Dahl¹²^ORCID,Lildballe Dorte Launholt²³,Hatt Lotte¹,Hedegaard Jakob¹,Singh Ripudaman¹^ORCID,Toft Christian Liebst Frisk⁴⁵^ORCID,Schelde Palle¹,Pedersen Anders Sune¹³,Knudsen Michael¹³,Vogel Ida²⁶

Affiliation:

1. ARCEDI Vejle Denmark

2. Center for Fetal Diagnostics, Department of Clinical Medicine Faculty of Health Aarhus University Aarhus Denmark

3. Department of Molecular Medicine Aarhus University Hospital Aarhus Denmark

4. Department of Molecular Diagnostics Aalborg University Hospital Aalborg Denmark

5. Center for Preimplantation Genetic Testing Aalborg University Hospital Aalborg Denmark

6. Department of Clinical Genetics Aarhus University Hospital Aarhus Denmark

Funder

Innovationsfonden

Novo Nordisk Fonden

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6276

Reference38 articles.

1. Hospital of Sick Children.Cystic Fibrosis Mutation Database [Internet]. [cited 2022 Mar 10].http://www.genet.sickkids.on.ca

2. The relative frequency of CFTR mutation classes in European patients with cystic fibrosis

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