Ana B. De La Hoz
Barakaldo, PV, Spain
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Correction: Genetic profile of a large Spanish cohort with hypercalcemia.
Journal: Frontiers in endocrinology
Published: October 23, 2025
Genetic profile of a large Spanish cohort with hypercalcemia.
Journal: Frontiers in endocrinology
Published: September 20, 2023
Five patients with disorders of calcium metabolism presented with GCM2 gene variants.
Journal: Scientific reports
Published: September 09, 2020
Novel variant in the CNNM2 gene associated with dominant hypomagnesemia.
Journal: PloS one
Published: May 27, 2020
Effect of AGG Interruptions on FMR1 Maternal Transmissions.
Journal: Frontiers in molecular biosciences
Published: April 28, 2020
Hereditary Spastic Paraplegia and Intellectual Disability: Clinicogenetic Lessons From a Family Suggesting a Dual Genetics Diagnosis.
Journal: Frontiers in neurology
Published: October 24, 2019
Molecular and Clinical Characterization of a Novel Nonsense Variant in Exon 1 of the UPF3B Gene Found in a Large Spanish Basque Family (MRX82).
Journal: Frontiers in genetics
Published: July 24, 2019
3p14 De Novo Interstitial Microdeletion in a Patient with Intellectual Disability and Autistic Features with Language Impairment: A Comparison with Similar Cases.
Journal: Case reports in genetics
Published: October 10, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026