Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sakineh Karimizare"'
Autor:
Mahin Hashemipour, Fahimeh Soheilipour, Sakineh Karimizare, Hossein Khanahmad, Morteza Karimipour, Sepideh Aminzadeh, Leila Kokabee, Massoud Amini, Silva Hovsepian, Rezvaneh Hadian
Publikováno v:
International Journal of Endocrinology, Vol 2012 (2012)
Background. Thyroid peroxidase gene (TPO) mutations are one of the most common causes of thyroid dyshormonogenesis in patients with congenital hypothyroidism (CH). In this study, the prevalence of TPO gene mutations in patients with thyroid dyshormon
Externí odkaz:
https://doaj.org/article/d528decbb8514d4c864c49b97ad88d2f
Autor:
Fahimeh Soheilipour, Sakineh Karimizare, Massoud Amini, Hossein Khanahmad, Morteza Karimipour, Mahin Hashemipour, Silva Hovsepian, Rezvaneh Hadian, Leila Kokabee, Sepideh Aminzadeh
Publikováno v:
Int J Endocrinol
Int J Endocrinol, 2012, 2012, pp.717283. ⟨10.1155/2012/717283⟩
International Journal of Endocrinology, Vol 2012 (2012)
International Journal of Endocrinology
Int J Endocrinol, 2012, 2012, pp.717283. ⟨10.1155/2012/717283⟩
International Journal of Endocrinology, Vol 2012 (2012)
International Journal of Endocrinology
Background. Thyroid peroxidase gene (TPO) mutations are one of the most common causes of thyroid dyshormonogenesis in patients with congenital hypothyroidism (CH). In this study, the prevalence of TPO gene mutations in patients with thyroid dyshormon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46c988166d5598943abda7b2f2c2802e
https://hal-riip.archives-ouvertes.fr/pasteur-00826038/document
https://hal-riip.archives-ouvertes.fr/pasteur-00826038/document
