PEKER, A. Et Al. 2022. Manifestations of a heterozygous CDK13 mutation as a rare entity; congenital heart defects, dysmorphic facial features, and intellectual developmental disorder. EURODYSMORPHO , (Barcelona, Spain).

PEKER, A., Karamık, G., COŞKUN, M., Öztürk, N., NUR, B., & MIHÇI, E., (2022). Manifestations of a heterozygous CDK13 mutation as a rare entity; congenital heart defects, dysmorphic facial features, and intellectual developmental disorder . EURODYSMORPHO, Barcelona, Spain

PEKER, ALP Et Al. "Manifestations of a heterozygous CDK13 mutation as a rare entity; congenital heart defects, dysmorphic facial features, and intellectual developmental disorder," EURODYSMORPHO, Barcelona, Spain, 2022

PEKER, ALP Et Al. "Manifestations of a heterozygous CDK13 mutation as a rare entity; congenital heart defects, dysmorphic facial features, and intellectual developmental disorder." EURODYSMORPHO , Barcelona, Spain, 2022

PEKER, A. Et Al. (2022) . "Manifestations of a heterozygous CDK13 mutation as a rare entity; congenital heart defects, dysmorphic facial features, and intellectual developmental disorder." EURODYSMORPHO , Barcelona, Spain.

@conferencepaper{conferencepaper, author={ALP PEKER Et Al. }, title={Manifestations of a heterozygous CDK13 mutation as a rare entity; congenital heart defects, dysmorphic facial features, and intellectual developmental disorder}, congress name={EURODYSMORPHO}, city={Barcelona}, country={Spain}, year={2022}}