Androgenetic chimerism as an etiology for Beckwith–Wiedemann syndrome: diagnosis and management-Reference-Cited by-同舟云学术

Androgenetic chimerism as an etiology for Beckwith–Wiedemann syndrome: diagnosis and management

Published:2019-11 Issue:11 Volume:21 Page:2644-2649
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Sheppard Sarah E.,Lalonde Emilie,Adzick N. Scott,Beck Anita E.,Bhatti Tricia,De Leon Diva D.,Duffy Kelly A.,Ganguly Arupa,Hathaway Evan,Ji Jianling,Linn Rebecca,Lord Katherine,Randolph Linda M.,Sajorda Brian,States Lisa,Conlin Laura K.,Kalish Jennifer M.

Funder

National Cancer Institute

Alex's Lemonade Stand Foundation for Childhood Cancer

St. Baldrick's Foundation

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/s41436-019-0551-9.pdf

Reference22 articles.

Cited by 15 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. Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes;Prenatal Diagnosis;2024-04

2. Should testing for mosaic genome-wide paternal uniparental disomy in Beckwith-Wiedemann spectrum (BWSp) be implemented in diagnostic testing?;European Journal of Human Genetics;2023-04-03

3. Mosaic genome‐wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells;American Journal of Medical Genetics Part A;2023-01-04

4. Placental Mesenchymal Dysplasia and Beckwith–Wiedemann Syndrome;Cancers;2022-11-12

5. Case report: Molecular analysis of a 47,XY,+21/46,XX chimera using SNP microarray and review of literature;Frontiers in Genetics;2022-11-11