Andrea P. Solari

Ministry Of Health, B, Argentina

Last Updated: 09/26/2026

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Found 8 publications

Classic Prader-Willi Syndrome Phenotype Caused by an Atypical Deletion in the 15q11 Region Not Involving the SNORD Genes.

Classic Prader-Willi Syndrome Phenotype Caused by an Atypical Deletion in the 15q11 Region Not Involving the SNORD Genes.

Journal: Clinical genetics

Published: November 28, 2024

Novel variant in the KAT6B gene associated with Say Barber Biesecker Young Simpson.

Novel variant in the KAT6B gene associated with Say Barber Biesecker Young Simpson.

Journal: Clinical dysmorphology

Published: August 30, 2023

TRIO-related intellectual disability with microcephaly: a case report of a patient with novel clinical findings.

TRIO-related intellectual disability with microcephaly: a case report of a patient with novel clinical findings.

Journal: Clinical dysmorphology

Published: October 10, 2020

Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.

Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.

Journal: Molecular biology reports

Published: February 03, 2020

Fragile X syndrome and other entities associated with the FMR1 gene: Study of 28 affected families

Fragile X syndrome and other entities associated with the FMR1 gene: Study of 28 affected families

Journal: Archivos argentinos de pediatria

Published: March 29, 2018

Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency.

Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency.

Journal: Genes

Published: May 21, 2017

16p11.2 Microdeletion: first report in Argentina

16p11.2 Microdeletion: first report in Argentina

Journal: Archivos argentinos de pediatria

Published: March 09, 2017

Structure-based activity prediction of CYP21A2 stability variants: A survey of available gene variations.

Structure-based activity prediction of CYP21A2 stability variants: A survey of available gene variations.

Journal: Scientific reports

Published: July 24, 2016

Showing 1-8 of 8

Last Updated: 09/26/2026