5 results on '"Bertucci, Emma"'
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2. Pre- and post-natal growth in two sisters with 3-M syndrome.
3. Fetal hepatic calcification in severe KAT6A (Arboleda-Tham) syndrome.
4. Autosomal recessive cutis laxa type IIIA: Report of a patient with severe phenotype and review of the literature.
5. Homozygous n.64C>T mutation in mitochondrial RNA-processing endoribonuclease gene causes cartilage hair hypoplasia syndrome in two siblings.
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