Peker, A. Et Al. 2022. Manifestations of aheterozygous CDK13 mutation as a rare entity; congenital hearth defects, dysmorphic facial features, and intellectual developmental disorder. ITHACA European Meeting On Dysmorphology , (Barcelona, Spain), 72-73.

Peker, A., Karamık, G., Coşkun, M., Öztürk, N., Yılmaz Bayer, Ö., Nur, B., ... Mıhçı, E.(2022). Manifestations of aheterozygous CDK13 mutation as a rare entity; congenital hearth defects, dysmorphic facial features, and intellectual developmental disorder . ITHACA European Meeting On Dysmorphology (pp.72-73). Barcelona, Spain

Peker, ALP Et Al. "Manifestations of aheterozygous CDK13 mutation as a rare entity; congenital hearth defects, dysmorphic facial features, and intellectual developmental disorder," ITHACA European Meeting On Dysmorphology, Barcelona, Spain, 2022

Peker, ALP Et Al. "Manifestations of aheterozygous CDK13 mutation as a rare entity; congenital hearth defects, dysmorphic facial features, and intellectual developmental disorder." ITHACA European Meeting On Dysmorphology , Barcelona, Spain, pp.72-73, 2022

Peker, A. Et Al. (2022) . "Manifestations of aheterozygous CDK13 mutation as a rare entity; congenital hearth defects, dysmorphic facial features, and intellectual developmental disorder." ITHACA European Meeting On Dysmorphology , Barcelona, Spain, pp.72-73.

@conferencepaper{conferencepaper, author={ALP PEKER Et Al. }, title={Manifestations of aheterozygous CDK13 mutation as a rare entity; congenital hearth defects, dysmorphic facial features, and intellectual developmental disorder}, congress name={ITHACA European Meeting On Dysmorphology}, city={Barcelona}, country={Spain}, year={2022}, pages={72-73} }