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Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: new highlights on phenotype-genotype correlations in Beckwith-Wiedemann syndrome.
Case 2 phenotype. (A-C) Frontal and lateral views showing severe omphalocoele and the dysmorphic features (short nose with anteverted nostrils, a long ...

J Med Genet
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