A. Rad Et Al. , "MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)," JOURNAL OF MEDICAL GENETICS , vol.56, no.5, pp.332-339, 2019
Rad, A. Et Al. 2019. MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome). JOURNAL OF MEDICAL GENETICS , vol.56, no.5 , 332-339.
Rad, A., Rad, A., Altunoglu, U., Altunoglu, U., Miller, R., Miller, R., ... Maroofian, R.(2019). MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome). JOURNAL OF MEDICAL GENETICS , vol.56, no.5, 332-339.
Rad, Abolfazl Et Al. "MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)," JOURNAL OF MEDICAL GENETICS , vol.56, no.5, 332-339, 2019
Rad, Abolfazl Et Al. "MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)." JOURNAL OF MEDICAL GENETICS , vol.56, no.5, pp.332-339, 2019
Rad, A. Et Al. (2019) . "MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)." JOURNAL OF MEDICAL GENETICS , vol.56, no.5, pp.332-339.
@article{article, author={Abolfazl Rad Et Al. }, title={MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)}, journal={JOURNAL OF MEDICAL GENETICS}, year=2019, pages={332-339} }