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Резултати

Prenatal diagnosis of RAG-deficient Omenn syndrome   [2000]

Villa, A; Bozzi, F; Sobacchi, Cristina; Strina, D; Fasth, A; Pasic, Srdjan S; Notarangelo, LD; Vezzoni, P

Maternal MTHFR 677C>T, 1298A>C gene polymorphisms and risk of offspring aneuploidy (✓)   [2022]

Miljanović, Olivera; Teofilov, Slađana; Anđelić, Miljana; Magić, Zvonko  ; Cikota‐Aleksić, Bojana  

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