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Noelia García-González

Observed name: García-González, Noelia
ORCID: 0000-0002-1085-0610
Observed ORCID: 0000-0002-1085-0610
OpenAlex ID: A5111165704
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Rubén Cabanillas, Marta Diñeiro, et al. · BMC Medical Genomics · 107
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Characterization of snRNA-related neurodevelopmental disorders through the Spanish Undiagnosed Rare Disease Programs
2025 · Marta Sevilla-Porras, Esther Nieto-Molina, et al. · medRxiv · 1
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Cerebral Cavernous Malformations
2021 · Igor Vázquez-Osorio, Noelia García-González, et al. · Indian Journal of Dermatology
Additional file 9: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Cabanillas, Rubén, Diñeiro, Marta, et al. · Figshare
Additional file 2: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Cabanillas, Rubén, Diñeiro, Marta, et al. · Figshare
Additional file 3: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Cabanillas, Rubén, Diñeiro, Marta, et al. · Figshare
Additional file 5: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Cabanillas, Rubén, Diñeiro, Marta, et al. · Figshare
Additional file 8: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Cabanillas, Rubén, Diñeiro, Marta, et al. · Figshare
Additional file 4: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Cabanillas, Rubén, Diñeiro, Marta, et al. · Figshare
Additional file 1: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Cabanillas, Rubén, Diñeiro, Marta, et al. · Figshare
Additional file 7: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Cabanillas, Rubén, Diñeiro, Marta, et al. · Figshare
Additional file 6: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
2018 · Cabanillas, Rubén, Diñeiro, Marta, et al. · Figshare
Works count: 13
Citation count: 108
H-index: 1
I10-index: 1
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