Literature DB >> 6606833

[Turner syndrome caused by deletion of the long arm of the X chromosome associated with adrenogenital syndrome caused by partial deficiency of 21-hydroxylase].

J L del Arbol, J A Soto Más, J A Fernández-Abril, J Raya Muñoz, F Martínez Tormo, J Gómez Rodríguez, J A Gómez Capilla, A Peña Yáñez.   

Abstract

Entities:  

Mesh：

Year:  1983        PMID： 6606833

Source DB:  PubMed          Journal:  Rev Clin Esp        ISSN： 0014-2565            Impact factor:   1.556


× No keyword cloud information.
  2 in total

1.  Turner syndrome with positive SRY gene and non-classical congenital adrenal hyperplasia: A case report.

Authors:  Mei-Nan He; Shan-Chao Zhao; Ji-Min Li; Lu-Lu Tong; Xin-Zhao Fan; Yao-Ming Xue; Xiao-Hong Lin; Ying Cao
Journal:  World J Clin Cases       Date:  2021-04-06       Impact factor: 1.337

2.  A rare combination: congenital adrenal hyperplasia due to 21 hydroxylase deficiency and Turner syndrome.

Authors:  Havva Nur Peltek Kendirci; Zehra Aycan; Semra Çetinkaya; Veysel Nijat Baş; Sebahat Yılmaz Ağladıoğlu; Aşan Önder
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-12
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.