New genetic and clinical evidence associated with fetal Beckwith–Wiedemann syndrome
Author:
Affiliation:
1. Department of Obstetrics and Gynecology Faculty of Medicine Chiang Mai University Meaung Chiang Mai Thailand
2. Department of Pediatrics Faculty of Medicine Chiang Mai University Meaung Chiang Mai Thailand
Funder
Chiang Mai University
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.5956
Reference24 articles.
1. Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement
2. Prevalence of Beckwith‐Wiedemann syndrome in North West of Italy;Mussa A;Am J Med Genet A,2013
3. Beckwith-Wiedemann Syndrome Presenting with an Elevated Triple Screen in the Second Trimester of Pregnancy
4. Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome
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3. Tandem Triplication 11p15.5-ICR1 (<i>H19/IGF2</i>) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case;Cytogenetic and Genome Research;2023-06-27
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