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Author/Creator Hoseini, Azadeh

1. Identification of a novel de novo variant in OTX2 in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosis. (4th March 2022)

Authors:
Rafati, Maryam; Mohamadhashem, Faezeh; Jalilian, Koosha; Hoseininasab, Fatemeh; Fakhri, Laya; Hoseini, Azadeh; Amiri, Hosna; Barati, Zeinab; Darzi Ramandi, Somayeh; Mostofinezhad, Nioosha; Mahmoudi, Amir Hosein; Ghaffari, Saeed Reza
Journal:
Ophthalmic genetics
Issue:
Volume 43:Number 2(2022)
Page Start:
262
Record Type:
Journal Article
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2. Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE‐diagnosis study (IMPRESsion). Issue 4 (3rd February 2022)

Authors:
Ghaffari, Saeed R.; Rafati, Maryam; Shadnoush, Mahdi; Pourbabaee, Shokooh; Aghighi, Mohammad; Mirab Samiee, Siamak; Kermanchi, Jamshid; Alaei, Mohammad R.; Salehpour, Shadab; Amirkashani, Davoud; Setoodeh, Aria; Sarkhail, Peymaneh; Badv, Reza Shervin; Aminzadeh, Majid; Shiva, Siamak; Eshraghi, Pe...
Journal:
Human mutation
Issue:
Volume 43:Issue 4(2022)
Page Start:
e1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗