Non‐invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysis-Reference-Cited by-同舟云学术

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Non‐invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysis

Published:2015-04-05 Issue:10 Volume:35 Page:950-958
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Hill Melissa¹²,Twiss Philip¹,Verhoef Talitha I.³,Drury Suzanne¹,McKay Fiona¹^ORCID,Mason Sarah¹,Jenkins Lucy¹,Morris Stephen³,Chitty Lyn S.¹²

Affiliation:

1. North East Thames Regional Genetics Service Great Ormond Street Hospital for Children NHS Foundation Trust London UK

2. Genetics and Genomic Medicine UCL Institute of Child Health and Great Ormond Street Hospital for Children NHS Trust London UK

3. Research Department of Applied Health Research University College London London UK

Funder

NIHR

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.4585

Reference33 articles.

1. A survey of newborn screening for cystic fibrosis in Europe

2. Cystic Fibrosis

3. Update on Procedure-Related Risks for Prenatal Diagnosis Techniques

4. Attitudes towards reproductive issues and carrier testing among adult patients and parents of children with cystic fibrosis (CF)

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2. Noninvasive Prenatal Genetic Screening of Cell-Free Fetal DNA for Early Prediction of β-Thalassemia Using Fiber Optic Nanogold-Linked Sorbent Assay;ACS Sensors;2024-08-01

3. Diagnosing Cystic Fibrosis in the 21st Century—A Complex and Challenging Task;Diagnostics;2024-04-03

4. Non-invasive prenatal testing: a revolutionary journey in prenatal testing;Frontiers in Medicine;2023-11-09

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