Pediatria
Saila
University of Bern
Berna, SuizaUniversity of Bern-ko ikertzaileekin lankidetzan egindako argitalpenak (5)
2024
2023
2019
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Broad Phenotypes of Disorders/Differences of Sex Development in MAMLD1 Patients Through Oligogenic Disease
Frontiers in Genetics, Vol. 10
2013
2006
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Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement
American Journal of Human Genetics, Vol. 79, Núm. 5, pp. 949-957