Publications

Rare Coexistence of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Turner Syndrome: A Case Report and Brief Literature Review

AuthID
P-00Y-560

Author(s)

Inacio, I

Serra Caetano, J

Cardoso, R

Dinis, I

Mirante, A

Document Type

Review

Year published

2023

Published

in JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, ISSN: 1308-5727

Volume: 15, Issue: 1, Pages: 86-89 (4)

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Wos^®

Pubmed^®

Google Scholar^®

Publication Identifiers

DOI: 10.4274/jcrpe.galenos.2021.2021.0174

Pubmed: 34355878

Wos: WOS:000938263200012

Source Identifiers

ISSN: 1308-5727

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Rare Coexistence of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Turner Syndrome: A Case Report and Brief Literature Review

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Rare Coexistence of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Turner Syndrome: A Case Report and Brief Literature Review

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