Karamık, G. Et Al. 2022. Novel Heterozygous missense mutation in the ski gene related Shprintzen-Goldberg Syndrome :A rare adult patient. ITHACA European Meeting On Dysmorphology , (Barcelona, Spain), 87-88.

Karamık, G., Öztürk, N., Yılmaz Bayer, Ö., Nur, B., & Mıhçı, E., (2022). Novel Heterozygous missense mutation in the ski gene related Shprintzen-Goldberg Syndrome :A rare adult patient . ITHACA European Meeting On Dysmorphology (pp.87-88). Barcelona, Spain

Karamık, GÖKCEN Et Al. "Novel Heterozygous missense mutation in the ski gene related Shprintzen-Goldberg Syndrome :A rare adult patient," ITHACA European Meeting On Dysmorphology, Barcelona, Spain, 2022

Karamık, GÖKCEN Et Al. "Novel Heterozygous missense mutation in the ski gene related Shprintzen-Goldberg Syndrome :A rare adult patient." ITHACA European Meeting On Dysmorphology , Barcelona, Spain, pp.87-88, 2022

Karamık, G. Et Al. (2022) . "Novel Heterozygous missense mutation in the ski gene related Shprintzen-Goldberg Syndrome :A rare adult patient." ITHACA European Meeting On Dysmorphology , Barcelona, Spain, pp.87-88.

@conferencepaper{conferencepaper, author={GÖKCEN KARAMIK Et Al. }, title={Novel Heterozygous missense mutation in the ski gene related Shprintzen-Goldberg Syndrome :A rare adult patient}, congress name={ITHACA European Meeting On Dysmorphology}, city={Barcelona}, country={Spain}, year={2022}, pages={87-88} }