A novel truncating variant in the FGD1 gene associated with Aarskog-Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly.

MLA

Kessel, Irena, et al. “A Novel Truncating Variant in the FGD1 Gene Associated with Aarskog-Scott Syndrome in a Family Previously Diagnosed with Tel Hashomer Camptodactyly.” American Journal of Medical Genetics. Part A, vol. 185, no. 10, Oct. 2021, pp. 3161–66. EBSCOhost, https://doi.org/10.1002/ajmg.a.62401.

APA

Kessel, I., German, A., Peleg, A., Gonzaga-Jauregui, C., Paperna, T., Ekhilevitch, N., Kurolap, A., Baris Feldman, H., & Sagi-Dain, L. (2021). A novel truncating variant in the FGD1 gene associated with Aarskog-Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly. American Journal of Medical Genetics. Part A, 185(10), 3161–3166. https://doi.org/10.1002/ajmg.a.62401

Chicago

Kessel, Irena, Alina German, Amir Peleg, Claudia Gonzaga-Jauregui, Tamar Paperna, Nina Ekhilevitch, Alina Kurolap, Hagit Baris Feldman, and Lena Sagi-Dain. 2021. “A Novel Truncating Variant in the FGD1 Gene Associated with Aarskog-Scott Syndrome in a Family Previously Diagnosed with Tel Hashomer Camptodactyly.” American Journal of Medical Genetics. Part A 185 (10): 3161–66. doi:10.1002/ajmg.a.62401.