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21
Lingual Fibrous Hyperplasia: Case Report and Literature Review
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22
Detection of the I172N Mutation in Cuban Patients with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Insufficiency
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23
Detección del polimorfismo p.K952L en pacientes cubanos con la enfermedad de Wilson
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24
Diagnóstico molecular de distrofia muscular de Duchenne/Becker en una familia sin antecedentes patológicos de la enfermedad
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25
Neurological manifestations associated with COVID-19 vaccine
Published 2025-01-01Subjects: Get full text
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