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Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3).
Rogers A, Nesbit MA, Hannan FM, Howles SA, Gorvin CM, Cranston T, Allgrove J, Bevan JS, Bano G, Brain C, Datta V, Grossman AB, Hodgson SV, Izatt L, Millar-Jones L, Pearce SH, Robertson L, Selby PL, Shine B, Snape K, Warner J, Thakker RV. Rogers A, et al. Among authors: shine b. J Clin Endocrinol Metab. 2014 Jul;99(7):E1300-5. doi: 10.1210/jc.2013-3909. Epub 2014 Apr 7. J Clin Endocrinol Metab. 2014. PMID: 24708097 Free PMC article.
Confusing genes: a patient with MEN2A and Cushing's disease.
Naziat A, Karavitaki N, Thakker R, Ansorge O, Sadler G, Gleeson F, Cranston T, McCormack A, Grossman AB, Shine B. Naziat A, et al. Among authors: shine b. Clin Endocrinol (Oxf). 2013 Jun;78(6):966-8. doi: 10.1111/cen.12072. Epub 2013 Apr 6. Clin Endocrinol (Oxf). 2013. PMID: 23072303 No abstract available.
Immunogenetics of Graves' ophthalmopathy.
Weetman AP, So AK, Warner CA, Foroni L, Fells P, Shine B. Weetman AP, et al. Among authors: shine b. Clin Endocrinol (Oxf). 1988 Jun;28(6):619-28. doi: 10.1111/j.1365-2265.1988.tb03853.x. Clin Endocrinol (Oxf). 1988. PMID: 2908181
152 results