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2021
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2022
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Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene.
Not available
S-EPMC8304864
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biostudies-literature
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High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis.
Not available
S-EPMC9605087
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biostudies-literature
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Pendred Syndrome, or Not Pendred Syndrome? That Is the Question.
Not available
S-EPMC8535891
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biostudies-literature
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