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You searched for: Author/Creator Romano, Roberta

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1. Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D TARDBP mutation. Issue 6 (16th December 2022)

3. DiGeorge‐like syndrome in a child with a 3p12.3 deletion involving MIR4273 gene born to a mother with gestational diabetes mellitus. Issue 7 (24th April 2017)

4. Epigenetics: An opportunity to shape innate and adaptive immune responses. Issue 4 (26th September 2022)