Kishi, H., Jojima, T., Kogai, T., Iijima, T., Ohira, E., Tanuma, D., . . . Aso, Y. (2020). A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation. Clin Case Rep.
Citação norma ChicagoKishi, Haruka, et al. "A Case of Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) Syndrome With a Novel Frameshift Variant in GATA3, P.W10Cfs40, Lacks Kidney Malformation." Clin Case Rep 2020.
Deismireacht MLAKishi, Haruka, et al. "A Case of Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) Syndrome With a Novel Frameshift Variant in GATA3, P.W10Cfs40, Lacks Kidney Malformation." Clin Case Rep 2020.
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