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Diana Miclea

Showing results (31-40 of 32) with videos related to

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Genes|January 21, 2023
Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the <i>GJB2</i> GeneAnca-Lelia Riza, Camelia Alkhzouz, Marius Farcaș, et al.
Diagnostics (Basel, Switzerland)|May 4, 2026
Molecular Diagnosis and Phenotypic Variability of Noonan Syndrome: Experience from a Romanian Multicenter StudyFlorina Victoria Nazarie, Mihaela Amelia Dobrescu, Cecilia Lazea, et al.
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Showing results (31-40 of 32) with videos related to

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Pageof 4
You have reached the last page of results.This site can display upto 32 results.
Genes|January 21, 2023
Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the <i>GJB2</i> GeneAnca-Lelia Riza, Camelia Alkhzouz, Marius Farcaș, et al.
Diagnostics (Basel, Switzerland)|May 4, 2026
Molecular Diagnosis and Phenotypic Variability of Noonan Syndrome: Experience from a Romanian Multicenter StudyFlorina Victoria Nazarie, Mihaela Amelia Dobrescu, Cecilia Lazea, et al.
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