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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Counseling and CYP1B1[original query]
CYP1B1 mutations in patients with primary congenital glaucoma from Saudi Arabia.
BMC medical genetics 2014 15 109.
Badeeb Osama M, Micheal Shazia, Koenekoop Robert K, den Hollander Anneke I, Hedrawi Manal
Phenotype and Genotype Correlation in Iranian Primary Congenital Glaucoma Patients.
Journal of glaucoma 2015 Jan .
Yazdani Shahin, Miraftabi Arezoo, Pakravan Mohammad, Ghahari Elham, Tousi Betsabeh K, Sedigh Massih, Yaseri Mehdi, Elahi Ela
A recurrent G367R mutation in MYOC associated with juvenile open angle glaucoma in a large Chinese family.
International journal of ophthalmology 2018 3 11 (3): 369-374.
Yao Yi-Hua, Wang Ya-Qin, Fang Wei-Fang, Zhang Liu, Yang Ju-Hua, Zhu Yi-H
Investigation of mutational spectrum in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma.
Pakistan journal of medical sciences 2023 3 39 (2): 409-416.
Zahid Tazeen, Khan Muhammad Umer, Zulfiqar Aymn, Jawad Fatima, Saleem Anosh, Khan Ahmad Ra
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