Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening-Reference-Cited by-同舟云学术

Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening

Published:2019-12 Issue:12 Volume:21 Page:2774-2780
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Brison Nathalie,Storms Jazz,Villela Darine,Claeys Kristl G.,Dehaspe Luc,de Ravel Thomy,De Waele Liesbeth,Goemans Nathalie,Legius Eric,Peeters Hilde,Van Esch Hilde,Race Valerie,Robert Vermeesch Joris,Devriendt Koenraad,Van Den Bogaert Kris

Funder

Fonds voor Wetenschappelijk Onderzoek

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/s41436-019-0564-4.pdf

Reference21 articles.

Cited by 20 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. Further evidence for an attenuated phenotype of in‐frame DMD deletions affecting the central rod domain of dystrophin around exon 48;American Journal of Medical Genetics Part A;2024-08-19

2. Prenatal risk assessment of Xp21.1 duplication involving theDMDgene by optical genome mapping;Life Science Alliance;2024-08-08

3. A new strategy for prenatal genetic screening of copy number variations in the DMD gene: A large cohort study based on NIPT analysis;Clinical and Translational Medicine;2024-05

4. Genetic counseling for the dystrophinopathies—Practice resource of the National Society of Genetic Counselors;Journal of Genetic Counseling;2024-04-29

5. Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles;European Journal of Human Genetics;2023-04-07