Yayıncı "Karger" Fen Edebiyat Fakültesi Koleksiyonu için listeleme
Toplam kayıt 2, listelenen: 1-2
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A Novel Mutation in the MC2R Gene Causing Familial Glucocorticoid Deficiency Type 1
(Karger, 2011)Familial glucocorticoid deficiency (FGD) or hereditary unresponsiveness to adrenocorticotropin (ACTH) is an autosomal recessive disorder characterized by isolated glucocorticoid deficiency associated with normal mineralocorticoid ... -
Thyroid Hormone Resistance Beta: Eighteen Pediatric Patient Experience
(Karger, 2018)[No Abstract Available]