Dyfyniad APA

Cangul, H., Liao, X., Schoenmakers, E., Kero, J., Barone, S., Srichomkwun, P., . . . Schoenmakers, N. (2018). Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism. JCI Insight.

Dyfyniad Arddull Chicago

Cangul, Hakan, et al. "Homozygous Loss-of-function Mutations in SLC26A7 Cause Goitrous Congenital Hypothyroidism." JCI Insight 2018.

Dyfyniad MLA

Cangul, Hakan, et al. "Homozygous Loss-of-function Mutations in SLC26A7 Cause Goitrous Congenital Hypothyroidism." JCI Insight 2018.

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