APA Alıntı

Almaghraby, A. (2019). MON-368 Familial Glucocorticoid Deficiency Type I with New MC2R Mutation: Presentation of a Pediatric Patient with Oral Mucosal Hyperpigmentation. J Endocr Soc.

Chicago Stili Alıntı

Almaghraby, Abdullah. "MON-368 Familial Glucocorticoid Deficiency Type I With New MC2R Mutation: Presentation of a Pediatric Patient With Oral Mucosal Hyperpigmentation." J Endocr Soc 2019.

MLA Alıntı

Almaghraby, Abdullah. "MON-368 Familial Glucocorticoid Deficiency Type I With New MC2R Mutation: Presentation of a Pediatric Patient With Oral Mucosal Hyperpigmentation." J Endocr Soc 2019.