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Roberta Milone

5PUBLICATIONS
4CO-AUTHORS
Cancer geneticsNeurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Neurogenetics
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Journal

Publications (5)

Sort by Publication Date:
|Jun 26, 2026
Expanding the Phenotypic Spectrum of Raynaud-Claes Syndrome: A Rett-like Presentation with Two New Cases.

|May 28, 2022
Enhancing <i>DLG2</i> Implications in Neuropsychiatric Disorders: Analysis of a Cohort of Eight Patients with 11q14.1 Imbalances.

Veronica Bertini, Roberta Milone, Paola Cristofani

|Nov 27, 2021
17q12 Recurrent Deletions and Duplications: Description of a Case Series with Neuropsychiatric Phenotype.

Roberta Milone, Raffaella Tancredi, Angela Cosenza

|Apr 03, 2021
De Novo 1q21.3q22 Duplication Revaluation in a "Cold" Complex Neuropsychiatric Case with Syndromic Intellectual Disability.

Roberta Milone, Roberta Scalise, Rosa Pasquariello

|Feb 23, 2019
A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture?

Roberta Milone, Riccardo Masson, Caterina Di Cosmo

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Frequent Collaborators

5 joint publications

Roberta Battini

1 joint publications

Silvano Bertelloni

1 joint publications

Alessandro Orsini

1 joint publications

Lorenza Marini

Frequent Collaborators

5 joint publications

Roberta Battini

1 joint publications

Silvano Bertelloni

1 joint publications

Alessandro Orsini

1 joint publications

Lorenza Marini