APA استشهاد

Haque, M. N., Kurata, K., Hosono, K., Ohtsubo, M., Ohishi, K., Sato, M., . . . Hotta, Y. (2019). A Japanese family with cone-rod dystrophy of delayed onset caused by a compound heterozygous combination of novel CDHR1 frameshift and known missense variants. Hum Genome Var.

استشهاد بنمط شيكاغو

Haque, Muhammad Nazmul, Kentaro Kurata, Katsuhiro Hosono, Masafumi Ohtsubo, Kentaro Ohishi, Miho Sato, Shinsei Minoshima, و Yoshihiro Hotta. "A Japanese Family With Cone-rod Dystrophy of Delayed Onset Caused By a Compound Heterozygous Combination of Novel CDHR1 Frameshift and Known Missense Variants." Hum Genome Var 2019.

MLA استشهاد

Haque, Muhammad Nazmul, et al. "A Japanese Family With Cone-rod Dystrophy of Delayed Onset Caused By a Compound Heterozygous Combination of Novel CDHR1 Frameshift and Known Missense Variants." Hum Genome Var 2019.

تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.