Pages that link to "Q36885699"
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The following pages link to Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome (Q36885699):
Displaying 8 items.
- Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele (Q37646069) (← links)
- Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases (Q42672527) (← links)
- 408 kb 15q11.2 microduplication by array comparative genomic hybridization in a fetus presenting with exomphalos, micrognathia, tetralogy of Fallot and normal karyotype: a genetic counseling dilemma in paternal carrier status (Q47833692) (← links)
- Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome (Q48048199) (← links)
- Virginal breast hypertrophy in a patient with Beckwith-Wiedemann syndrome. (Q52358154) (← links)
- Jacobsen and Beckwith-Wiedemann syndromes in a child with mosaicism for partial 11pter trisomy and partial 11qter monosomy. (Q53124535) (← links)
- Immunohistochemical expression of p57 in placental vascular proliferative disorders of preterm and term placentas. (Q54776822) (← links)
- Accuracy and impact of prenatal diagnosis in infants with omphalocele. (Q55245863) (← links)