Martina Busè

4PUBLICATIONS
8CO-AUTHORS
Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Neonatology
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Publications (4)

|Jul 30, 2020
12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: a case report and review of the literature.

Francesca Mercadante, Martina Busè, Emanuela Salzano

|May 17, 2018
Inhaled nitric oxide as a rescue therapy in a preterm neonate with severe pulmonary hypertension: a case report.

Martina Busè, Francesco Graziano, Fabio Lunetta

|Jul 21, 2017
Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series.

Martina Busè, Helenia C Cuttaia, Daniela Palazzo

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