B. TÜYSÜZ Et Al. , "Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes," JOURNAL OF MEDICAL GENETICS , 2022
TÜYSÜZ, B. Et Al. 2022. Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes. JOURNAL OF MEDICAL GENETICS .
TÜYSÜZ, B., ULUDAĞ ALKAYA, D., Geyik, F., ALAYLIOĞLU, M., Kasap, B., KURUĞOĞLU, S., ... Akman, Y. E.(2022). Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes. JOURNAL OF MEDICAL GENETICS .
TÜYSÜZ, BEYHAN Et Al. "Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes," JOURNAL OF MEDICAL GENETICS , 2022
TÜYSÜZ, BEYHAN Et Al. "Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes." JOURNAL OF MEDICAL GENETICS , 2022
TÜYSÜZ, B. Et Al. (2022) . "Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes." JOURNAL OF MEDICAL GENETICS .
@article{article, author={BEYHAN TÜYSÜZ Et Al. }, title={Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes}, journal={JOURNAL OF MEDICAL GENETICS}, year=2022}