Maria Ramos-Arroyo

5PUBLICATIONS
38CO-AUTHORS
Educational counsellingPredictive and prognostic markersNeurogeneticsDisease surveillance
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Publications (5)

|Nov 20, 2024
Prognostic significance of mutation type and chromosome fragility in Fanconi anemia.

María José Ramírez, Roser Pujol, Jordi Minguillón

|Mar 03, 2024
Somatic CAG repeat instability in intermediate alleles of the HTT gene and its potential association with a clinical phenotype.

Ainara Ruiz de Sabando, Marc Ciosi, Arkaitz Galbete

|Sep 21, 2022
Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington disease.

Ainara Ruiz de Sabando, Edurne Urrutia Lafuente, Arkaitz Galbete

|Feb 11, 2021
Validation of diagnostic codes and epidemiologic trends of Huntington disease: a population-based study in Navarre, Spain.

Esther Vicente, Ainara Ruiz de Sabando, Fermín García

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