Search Results - Michela Malacarne

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  1. 1
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    12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: a case report and review of the literature by Francesca Mercadante, Martina Busè, Emanuela Salzano, Tiziana Fragapane, Daniela Palazzo, Michela Malacarne, Maria Piccione

    Published 2020
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  2. 2
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    Children and adults affected by Cri du Chat syndrome: Care's recommendations by Maria Elena Liverani, Alice Spano, Cesare Danesino, Michela Malacarne, Simona Cavani, Marianna Spunton, Andrea Guala

    Published 2019
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    Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series by Martina Busè, Helenia C. Cuttaia, Daniela Palazzo, Marcella V. Mazara, Salvatrice A. Lauricella, Michela Malacarne, Mauro Pierluigi, Simona Cavani, Maria Piccione

    Published 2017
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