References
- Katari S, Wood-Trageser MA, Jiang H, et al. Novel inactivating mutation of the FSH receptor in two siblings of Indian origin with premature ovarian failure. J Clin Endocrinol Metab. 2015;100:2154–2157.
- Kovanci E, Schutt AK. Premature ovarian failure: clinical presentation and treatment. Obstet Gynecol Clin North Am. 2015;42:153–161.
- Caburet S, Arboleda VA, Llano E, et al. Mutant cohesin in premature ovarian failure. N Engl J Med. 2014;370:943–949.
- Ou Z, Li S, Li Q, et al. Duchenne muscular dystrophy in a female patient with a karyotype of 46,X,i(X)(q10). Tohoku J Exp Med. 2010;222:149–153.
- Laundon CH, Spencer K, Macri JN, et al. Free beta hCG screening of hydropic and non-hydropic Turner syndrome pregnancies. Prenat Diagn. 1996;16:853–856.
- Yeh T, Soto AG, Quintos JB, et al. Turner syndrome and pituitary adenomas: a case report and review of literature. J Pediatr Endocrinol Metab. 2017;30:231–235.
- Kara C, Ustyol A, Yilmaz A, et al. Premature ovarian failure due to tetrasomy X in an adolescent girl. Eur J Pediatr. 2014;173:1627–1630.
- Vichinsartvichai P, Manolertthewan C, Promrungrueng P. Premature ovarian failure with 46,XX,t(1;4)(p34.1;q34): first case report and literature review. Climacteric. 2015;18:656–658.
- Colao E, Granata T, Vismara MF, et al. A case of premature ovarian failure in a 33-year-old woman. Case Rep Genet. 2013;2013:573841.
- Dittmar M, Kahaly GJ. Genetics of the autoimmune polyglandular syndrome type 3 variant. Thyroid. 2010;20:737–743.
- Jankowska K. Premature ovarian failure. Prz Menopauzalny. 2017;16:51–56.
- Kim D. The role of vitamin D in thyroid diseases. Int J Mol Sci. 2017;18:1949.