Search Results - Yakicier, Mustafa C.

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  1. 1
    SIP1 is downregulated in hepatocellular carcinoma by promoter hypermethylation

    SIP1 is downregulated in hepatocellular carcinoma by promoter hypermethylation by Acun, Tolga, Oztas, Emin, Yagci, Tamer, Yakicier, Mustafa C

    Published in BMC cancer
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  2. 2
    Injectable tissue-engineered cartilage using commercially available fibrin glue

    Injectable tissue-engineered cartilage using commercially available fibrin glue by Cakmak, Ozcan, Babakurban, Seda T., Akkuzu, Hatice G., Bilgi, Selcuk, Ovalı, Ercüment, Kongur, Merve, Altintas, Hande, Yilmaz, Bayram, Bilezikçi, Banu, Y. Celik, Zerrin, Yakicier, Mustafa C., Sahin, Feride I.

    Published in The Laryngoscope
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  3. 3
    A case of pulmonary alveolar microlithiasis associated with a homozygous 195 kb deletion encompassing the entire SLC34A2 gene

    A case of pulmonary alveolar microlithiasis associated with a homozygous 195 kb deletion encompassing the entire SLC34A2 gene by Stokman, Lara, Nossent, Esther J., Grunberg, Katrien, Meijboom, Lilian, Yakicier, Mustafa C., Voorhoeve, Els, Houweling, Arjan C.

    Published in Clinical case reports
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  4. 4
    A case of pulmonary alveolar microlithiasis associated with a homozygous 195 kb deletion encompassing the entire SLC 34A2 gene

    A case of pulmonary alveolar microlithiasis associated with a homozygous 195 kb deletion encompassing the entire SLC 34A2 gene by Stokman, Lara, Nossent, Esther J., Grunberg, Katrien, Meijboom, Lilian, Yakicier, Mustafa C., Voorhoeve, Els, Houweling, Arjan C.

    Published in Clinical case reports
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  5. 5
    A case of pulmonary alveolar microlithiasis associated with a homozygous 195 kb deletion encompassing the entire SLC34A2 gene

    A case of pulmonary alveolar microlithiasis associated with a homozygous 195 kb deletion encompassing the entire SLC34A2 gene by Stokman, Lara, Nossent, Esther J, Grunberg, Katrien, Meijboom, Lilian, Yakicier, Mustafa C, Voorhoeve, Els, Houweling, Arjan C

    Published in Clinical case reports
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  6. 6
    Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate

    Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate by Breckpot, Jeroen, Anderlid, Britt-Marie, Alanay, Yasemin, Blyth, Moira, Brahimi, Afane, Duban-Bedu, Bénédicte, Gozé, Odile, Firth, Helen, Yakicier, Mustafa Cengiz, Hens, Greet, Rayyan, Maissa, Legius, Eric, Vermeesch, Joris Robert, Devriendt, Koen

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