Autosomal recessive cutis laxa: a novel mutation in the FBLN5 gene in a family

MLA

İbrahim Tekedereli, et al. “Autosomal Recessive Cutis Laxa: A Novel Mutation in the FBLN5 Gene in a Family.” Clinical Dysmorphology, vol. 28, Apr. 2019, pp. 63–65. EBSCOhost, https://doi.org/10.1097/mcd.0000000000000258.

APA

İbrahim Tekedereli, Ismail Kursad Gokce, Emine Demiral, Zeynep Esener, Ayşehan Akıncı, & Emine Çamtosun. (2019). Autosomal recessive cutis laxa: a novel mutation in the FBLN5 gene in a family. Clinical Dysmorphology, 28, 63–65. https://doi.org/10.1097/mcd.0000000000000258

Chicago

İbrahim Tekedereli, Ismail Kursad Gokce, Emine Demiral, Zeynep Esener, Ayşehan Akıncı, and Emine Çamtosun. 2019. “Autosomal Recessive Cutis Laxa: A Novel Mutation in the FBLN5 Gene in a Family.” Clinical Dysmorphology 28 (April): 63–65. doi:10.1097/mcd.0000000000000258.