Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Counseling and CYP11B1[original query] |
---|
Novel and prevalent CYP11B1 gene mutations in Turkish patients with 11-ß hydroxylase deficiency. The Journal of steroid biochemistry and molecular biology 2016 Mar . Kandemir Nurgun, Yilmaz Didem Yucel, Gonc E Nazli, Ozon Alev, Alikasifoglu Ayfer, Dursun Ali, Ozgul R Koks |
Prevalence, clinical characteristics and long-term outcomes of classical 11 ?-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene. The Journal of steroid biochemistry and molecular biology 2018 4 181 88-97. Ba? Firdevs, Toksoy Güven, Ergun-Longmire Berrin, Uyguner Zehra Oya, Abal? Zehra Yava?, Poyrazo?lu ?ükran, Karaman Volkan, Avc? ?ahin, Altuno?lu Umut, Bundak Ruveyde, Karaman Birsen, Ba?aran Seher, Darendeliler Fey |
Giant bilateral adrenal myelolipomas in two Chinese families with congenital adrenal hyperplasia. Endocrine connections 2018 10 7 (11): 1136-41. Liu Qiuli, Wang Lin-Ang, Su Jian, Tong Dali, Lan Weihua, Wang Luofu, Liu Gaolei, Zhang Jun, Zhang Victor Wei, Zhang Dianzheng, Chen Rongrong, Zhu Qingyi, Jiang J |
- Page last reviewed:Feb 1, 2024
- Content source: