Results 191 to 200 of about 4,073 (218)
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[Analysis of CYP21A2 gene mutation in one case of congenital adrenal hyperplasia].
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2014CYP21A2 gene mutations in a child with congenital adrenal hyperplasia (CAH), and the child's parents, were detected in the study. The clinical features, treatment monitoring and molecular genetic mechanism of CAH are reviewed. In the study, DNA was extracted from peripheral blood samples using the QIAGEN Blood DNA Mini Kit; a highly specific PCR primer
Xiao-Mei, Lin +8 more
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Cancer epigenetics in clinical practice
Ca-A Cancer Journal for Clinicians, 2023Veronica Davalos, Manel Esteller
exaly
Horizontal gene transfer and adaptive evolution in bacteria
Nature Reviews Microbiology, 2021Brian J Arnold, William P Hanage
exaly
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia.
Human genetics, 2010Ettore, Capoluongo +3 more
openaire +1 more source
Functional importance of novel nucleotide variations in the CYP21A2 gene
2021openaire +1 more source
Nanooncology: The future of cancer diagnosis and therapy
Ca-A Cancer Journal for Clinicians, 2013Sanjiv S Gambhir
exaly