B. Tüysüz Et Al. , "Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.," European journal of medical genetics , vol.64, no.12, pp.104346, 2021
Tüysüz, B. Et Al. 2021. Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.. European journal of medical genetics , vol.64, no.12 , 104346.
Tüysüz, B., Alp Ünkar, Z., Turan, H., Gezdirici, A., Uludağ Alkaya, D., Kasap, B., ... Yeşil, G.(2021). Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.. European journal of medical genetics , vol.64, no.12, 104346.
Tüysüz, Beyhan Et Al. "Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.," European journal of medical genetics , vol.64, no.12, 104346, 2021
Tüysüz, Beyhan Et Al. "Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.." European journal of medical genetics , vol.64, no.12, pp.104346, 2021
Tüysüz, B. Et Al. (2021) . "Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.." European journal of medical genetics , vol.64, no.12, p.104346.
@article{article, author={Beyhan Tüysüz Et Al. }, title={Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.}, journal={European journal of medical genetics}, year=2021, pages={104346} }