Sarac Sivrikoz, T. Et Al. 2022. Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center.. Archives of gynecology and obstetrics , vol.305, no.2 , 323-342.

Sarac Sivrikoz, T., Basaran, S., Has, R., Karaman, B., Kalelioglu, I. H., Kirgiz, M., ... Altunoglu, U.(2022). Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center.. Archives of gynecology and obstetrics , vol.305, no.2, 323-342.

Sarac Sivrikoz, Tuğba Et Al. "Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center.," Archives of gynecology and obstetrics , vol.305, no.2, 323-342, 2022

Sarac Sivrikoz, Tuğba S. Et Al. "Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center.." Archives of gynecology and obstetrics , vol.305, no.2, pp.323-342, 2022

Sarac Sivrikoz, T. Et Al. (2022) . "Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center.." Archives of gynecology and obstetrics , vol.305, no.2, pp.323-342.

@article{article, author={Tuğba SARAÇ SİVRİKOZ Et Al. }, title={Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center.}, journal={Archives of gynecology and obstetrics}, year=2022, pages={323-342} }