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Results: 1-4 |
Results: 4
A missense mutation encoding Cys(67) -> Gly in neurophysin II is associated with early onset autosomal dominant neurohypophyseal diabetes insipidus
Authors: DiMeglio, LA Gagliardi, PC Browning, JE Quigley, CA Repaske, DR
Citation: La. Dimeglio et al., A missense mutation encoding Cys(67) -> Gly in neurophysin II is associated with early onset autosomal dominant neurohypophyseal diabetes insipidus, MOL GEN MET, 72(1), 2001, pp. 39-44
Development of a congenital hypothyroidism follow-up program - The Indianaexperience
Authors: Eugster, EA Pescovitz, OH Quigley, CA Johnson, N Rivkees, SA
Citation: Ea. Eugster et al., Development of a congenital hypothyroidism follow-up program - The Indianaexperience, ENDOCRINOLO, 10(3), 2000, pp. 185-193
Hypogonadism and CHARGE association
Authors: Wheeler, PG Quigley, CA Sadeghi-Nejad, A Weaver, DD
Citation: Pg. Wheeler et al., Hypogonadism and CHARGE association, AM J MED G, 94(3), 2000, pp. 228-231
The contribution of testosterone to skeletal development and maintenance: Lessons from the androgen insensitivity syndrome
Authors: Marcus, R Leary, D Schneider, DL Shane, E Favus, M Quigley, CA
Citation: R. Marcus et al., The contribution of testosterone to skeletal development and maintenance: Lessons from the androgen insensitivity syndrome, J CLIN END, 85(3), 2000, pp. 1032-1037
Risultati: 1-4 |