Improving the prenatal diagnosis of Beckwith–Wiedemann syndrome
Author:
Affiliation:
1. Department of Obstetrics and Gynecology Baylor College of Medicine Houston Texas USA
2. Department of Molecular and Human Genetics Baylor College of Medicine Houston Texas USA
3. Texas Children’s Hospital Houston Texas USA
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.5971
Reference13 articles.
1. Omphalocele—What should we tell the prospective parents?
2. Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement
3. Prenatally diagnosed omphaloceles: Report of 92 cases and association with Beckwith‐Wiedemann syndrome
4. The diagnostic potential of targeted imaging of the fetal pancreas
5. New genetic and clinical evidence associated with fetal Beckwith–Wiedemann syndrome
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. Beckwith-Wiedemann syndrome in a child with multifocal Wilms tumor and lateralized overgrowth: A case report;Radiology Case Reports;2023-09
2. Turner syndrome‐omphalocele association: Incidence, karyotype, phenotype and fetal outcome;Prenatal Diagnosis;2023-01-31
3. Proposal for Practical Approach in Prenatal Diagnosis of Beckwith–Wiedemann Syndrome and Review of the Literature;Diagnostics;2022-07-13
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