Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Counseling and CYP21A1P[original query] |
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Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations. Journal of endocrinological investigation 2015 Aug . Milacic I, Barac M, Milenkovic T, Ugrin M, Klaassen K, Skakic A, Jesic M, Joksic I, Mitrovic K, Todorovic S, Vujovic S, Pavlovic S, Stojiljkovic |
p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche. International journal of endocrinology 2020 7 2020 4329791. Soveizi Mahdieh, Mahdieh Nejat, Setoodeh Aria, Sayarifard Fatemeh, Abbasi Farzaneh, Bose Himangshu S, Rabbani Bahareh, Rabbani A |
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