Identification of a Novel Homozygous INSR Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates.

MLA

Bastaki, Fatma, et al. “Identification of a Novel Homozygous INSR Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates.” Hormone Research in Paediatrics, vol. 87, no. 1, Feb. 2017, pp. 64–68. EBSCOhost, https://doi.org/10.1159/000447090.

APA

Bastaki, F., Nair, P., Mohamed, M., Khadora, M. M., Saif, F., Tawfiq, N., al-ali, M. T., & Hamzeh, abdul R. (2017). Identification of a Novel Homozygous INSR Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates. Hormone Research in Paediatrics, 87(1), 64–68. https://doi.org/10.1159/000447090

Chicago

Bastaki, Fatma, Pratibha Nair, Madiha Mohamed, Manal Mustafa Khadora, Fatima Saif, Nafisa Tawfiq, Mahmoud Taleb al-ali, and abdul Rezzak Hamzeh. 2017. “Identification of a Novel Homozygous INSR Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates.” Hormone Research in Paediatrics 87 (1): 64–68. doi:10.1159/000447090.