Suchergebnisse - "Kezuka, Atsumi"

PubPharm (3)

1

A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation

enthalten in: Clinical case reports | 2020

von Kishi, H. | Jojima, T. | Kogai, T. | +13

2

Genetic alteration of ARMC5 in a patient diagnosed with meningioma and primary macronodular adrenal hyperplasia : a case report

enthalten in: European journal of endocrinology | 2020

von Jojima, T. | Kogai, T. | Iijima, T. | +13

3

A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation

enthalten in: Clinical Case Reports | 2020

von Kishi, H. | Jojima, T. | Kogai, T. | +13

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