Pretraga




Rezultati

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

Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy-Walker malformation and single ventricle heart   [2024]

Stankovic, Andjela; Toljic, Mina; Karadzov-Orlic, Natasa T; Mikovic, Zeljko M; Joksic, Ivana D

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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