Genotype-Phenotype Correlation in Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency in Cuba

BACKGROUND: There are several studies that show a good genotype-phenotype correlation in congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD). However, there is well-documented evidence of inconsistency in some cases. OBJECTIVES: To determine if there is a correlation betwee...

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Bibliografiset tiedot
Julkaisussa:Int J Endocrinol
Päätekijät: Espinosa Reyes, Tania Mayvel, Collazo Mesa, Teresa, Lantigua Cruz, Paulina Arasely, Agramonte Machado, Adriana, Domínguez Alonso, Emma, Falhammar, Henrik
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi 2021
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7806372/
https://ncbi.nlm.nih.gov/pubmed/33505466
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2021/9316284
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