Correspondence on “Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions” by Hoskovec et al-Reference-Cited by-同舟云学术

Correspondence on “Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions” by Hoskovec et al

Published:2023-09 Issue:9 Volume:25 Page:100902
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Benn Peter^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference10 articles.

1. Genetic disorders in children and young adults: a population study;Baird;A J Hum Genet,1988

2. Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG);Gregg;Genet Med,2021

3. An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals;Lazarin;Genet Med,2013

4. Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach;Westemeyer;Genet Med,2020

5. Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions;Hoskovec;Genet Med,2023

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Reproductive Carrier Screening: Identifying Families at Risk for Familial Hypercholesterolemia in the United States;Circulation: Genomic and Precision Medicine;2024-04

2. Single gene non‐invasive prenatal testing when the father is not available for testing; concerns regarding Wynn et al., Prenatal Diagnosis 2023. 43:1344–54;Prenatal Diagnosis;2023-11-22

3. Response to Benn et al;Genetics in Medicine;2023-09