6 results on '"Özçelik, Tayfun"'
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2. Recessive LAMC3 mutations cause malformations of occipital cortical development
3. Collaborative genomics for human health and cooperation in the Mediterranean region
4. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region
5. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region
6. Molecular evolution of the human interleukin–8 receptor gene cluster
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