Grati, F. R., Turolla, L., D'Ajello, P., Ruggeri, A., Miozzo, M., Bracalente, G., . . . Simoni, G. (2007). Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: New highlights on phenotype–genotype correlations in Beckwith–Wiedemann syndrome. BMJ Group.
Chicago-стиль цитированияGrati, F R., et al. Chromosome 11 Segmental Paternal Isodisomy in Amniocytes From Two Fetuses With Omphalocoele: New Highlights On Phenotype–genotype Correlations in Beckwith–Wiedemann Syndrome. BMJ Group, 2007.
MLA-цитированиеGrati, F R., et al. Chromosome 11 Segmental Paternal Isodisomy in Amniocytes From Two Fetuses With Omphalocoele: New Highlights On Phenotype–genotype Correlations in Beckwith–Wiedemann Syndrome. BMJ Group, 2007.