The Clinical and Molecular Characterization of Patients With Dyshormonogenic Congenital Hypothyroidism Reveals Specific Diagnostic Clues for DUOX2 Defects
Muzza, M, Rabbiosi, S, Vigone, M. C, Zamproni, I, Cirello, V, Maffini, M. A, Maruca, K, Schoenmakers, N, Beccaria, L, Gallo, F, Park, S.-M, Beck-Peccoz, P, Persani, L, Weber, G, Fugazzola, L
Published in The journal of clinical endocrinology and metabolism (01.03.2014)
Published in The journal of clinical endocrinology and metabolism (01.03.2014)
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Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3
Elli, F M, deSanctis, L, Maffini, M A, Bordogna, P, Tessaris, D, Pirelli, A, Arosio, M, Linglart, A, Mantovani, G
Published in Clinical epigenetics (07.01.2019)
Published in Clinical epigenetics (07.01.2019)
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