Diagnostic limitations of routine low-coverage CNV-seq in detecting mosaic paternal uniparental disomy in Beckwith-Wiedemann syndrome: a case report. [PDF]
Li M, Luo L, Jiao J, Cheng Y.
europepmc +1 more source
[Giant omphalocele: a clinical case].
C, Yurác +4 more
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Prenatal Diagnosis and Perinatal Management Considerations in Congenital Abdominal Wall Defects: A Case Series and Narrative Review. [PDF]
Popovski N, Stoyanova N, Caiulo R.
europepmc +1 more source
Prenatal and Postnatal Determinants of Outcome in Neonates with Omphalocele: A 25-Year Single-Center Cohort Study. [PDF]
Namat DA +9 more
europepmc +1 more source
Enhancing rare disease guideline development with real-world data: a method evaluation. [PDF]
Irvine W +7 more
europepmc +1 more source
Patient-Reported Long-Term Gastrointestinal Outcomes in Children with Omphalocele and Gastroschisis: A PedsQL GI Module Study. [PDF]
Hogerwerf M +6 more
europepmc +1 more source
Rare Association of Type 1 Omphalocele With Ileocecal Atresia and Congenital Appendiceal Agenesis: A Case Report. [PDF]
Mellouki MT +3 more
europepmc +1 more source
Congenital stomised omphalocele: a case report and scoping literature review. [PDF]
Loria G +5 more
europepmc +1 more source
Clinical application and systematic review of waiting treatment for giant omphaloceles. [PDF]
Pan R +8 more
europepmc +1 more source
Prenatal diagnosis of giant omphalocele on ultrasonography
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