Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marziyeh Hoseinzadeh"'
Autor:
Aliasgar Mohammadi, Marziyeh Hoseinzadeh, Sina Narrei, Mohammad Reza Pourreza, Yousof Mohammadi, Mahnaz Norouzi, Ladan Sadeghian, Mohammad Amin Tabatabaiefar
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-8 (2024)
Abstract Background Sensorineural hearing loss (SNHL) is a clinically and genetically heterogeneous group of disorders of the auditory system. SNHL can occur as a symptom in more than 400 syndromes, and mutations in more than 150 genes can lead to SN
Externí odkaz:
https://doaj.org/article/b98c4e75825f442c92fc2d8bd2454865
Autor:
Shahrzad Aghaei, Effat Farrokhi, Javad saffari-chaleshtori, Marziyeh Hoseinzadeh, Newsha Molavi, Mahin Hashemipour, Noushin Rostampour, Samira Asgharzadeh, Mohammad Amin Tabatabaiefar
Publikováno v:
Molecular Genetics and Genomics. 298:693-708
Autor:
Shahrzad Aghaei, Sepideh Parvizpour, Effat Farrokhi, Newsha Molavi, Marziyeh Hoseinzadeh, Mohammad Amin Tabatabaiefar
Publikováno v:
Journal of Biomolecular Structure and Dynamics. :1-15
Androgen insensitivity syndrome (AIS) is a common form of 46, XY disorder in sex development disease (DSD). It is due to the androgen receptor (
Autor:
Marziyeh Hoseinzadeh, Newsha Molavi, Mahnaz Norouzi, Shahrzad Aghaei, Mehrdad Zeinalian, Mahin Hashemipour, Mohammad Amin Tabatabaiefar
Publikováno v:
Laboratory medicine.
Objective Congenital adrenal hyperplasia (CAH) addresses a number of autosomal recessive disorders characterized by the enzyme defects in steroid hormones biosynthesis. The second common form of CAH is caused by mutations in the CYP11B1 gene. Here, w