Paola Concolino

10PUBLICATIONS
0CO-AUTHORS
Developmental genetics (incl. sex determination)Cancer geneticsCancer diagnosisNeonatologyGene expression (incl. microarray and other genome-wide approaches)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (10)

|Feb 07, 2024
Chimeric Genes Causing 11β-Hydroxylase Deficiency: Implications in Clinical and Molecular Diagnosis.

Paola Concolino

|Aug 07, 2023
Genetic Characterization of a Cohort of Italian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Paola Concolino, Alessia Perrucci, Cinzia Carrozza

|Apr 27, 2022
CAH-X Syndrome: Genetic and Clinical Profile.

Paola Concolino, Henrik Falhammar

|Mar 12, 2021
Molecular Analysis of 21-Hydroxylase Deficiency Reveals Two Novel Severe Genotypes in Affected Newborns.

Paola Concolino, Rosa Maria Paragliola

|Jul 02, 2020
A Novel Pathogenic Variant in the N-Terminal Domain of the Glucocorticoid Receptor, Causing Glucocorticoid Resistance.

Rosa Maria Paragliola, Alessandra Costella, Andrea Corsello

|Jul 19, 2019
Issues with the Detection of Large Genomic Rearrangements in Molecular Diagnosis of 21-Hydroxylase Deficiency.

Paola Concolino

Pageof 2

Frequent Collaborators