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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 1 phenotype. (A, B) Frontal view showing body asymmetry with hemihypertrophy of the right body side, omphalocoele, short nose with anteverted ...

J Med Genet
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