Andrea Vitale

发表

Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome

G. Limongelli, L. Pastore, V. D’Argenio, 2020, Molecular genetics & genomic medicine.

D-aspartate oxidase gene duplication induces social recognition memory deficit in mice and intellectual disabilities in humans

A. Usiello, E. Leggiero, L. Pastore, 2022, Translational Psychiatry.

Identification of a De Novo Deletion by Using A-CGH Involving PLNAX2: An Interesting Candidate Gene in Psychomotor Developmental Delay

L. Pastore, B. Lombardo, Annaluisa Ranieri, 2022, Medicina.

Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss

P. Gasparini, A. D’Amico, A. d'Adamo, 2015, Molecular Cytogenetics.

Intragenic Deletion in MACROD2: A Family with Complex Phenotypes Including Microcephaly, Intellectual Disability, Polydactyly, Renal and Pancreatic Malformations

L. Pastore, V. Costa, C. Perrotta, 2019, Cytogenetic and Genome Research.

CGH array for the identification of a compound heterozygous mutation in the CYP1B1 gene in a patient with bilateral anterior segment dysgenesis

E. Leggiero, L. Pastore, C. Perrotta, 2018, Clinical chemistry and laboratory medicine.

3q29 microduplication in a small family with complex metabolic phenotype from Southern Italy

L. Pastore, F. Pasanisi, P. Buono, 2018, Clinical chemistry and laboratory medicine.

Two novel genomic rearrangements identified in suicide subjects using a-CGH array

V. Carli, M. Sarchiapone, L. Pastore, 2015, Clinical chemistry and laboratory medicine.

Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss

P. Gasparini, A. D’Amico, A. d'Adamo, 2015, Molecular Cytogenetics.