ROSA MARÍA MARTÍNEZ SALAZAR-rekin lankidetzan egindako argitalpenak (2)
2020
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Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?
Frontiers in Endocrinology, Vol. 11
2019
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Variable phenotype in HNF1B mutations: Extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract
Clinical Kidney Journal, Vol. 12, Núm. 3, pp. 373-379