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Author/Creator Nikzat, Nooshin

1. Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. Issue 12 (7th October 2015)

Authors:
Sloan-Heggen, Christina M; Babanejad, Mojgan; Beheshtian, Maryam; Simpson, Allen C; Booth, Kevin T; Ardalani, Fariba; Frees, Kathy L; Mohseni, Marzieh; Mozafari, Reza; Mehrjoo, Zohreh; Jamali, Leila; Vaziri, Saeideh; Akhtarkhavari, Tara; Bazazzadegan, Niloofar; Nikzat, Nooshin; Arzhangi, Sanaz; S...
Journal:
Journal of medical genetics
Issue:
Volume 52:Issue 12(2015)
Page Start:
823
Record Type:
Journal Article
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2. Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran. Issue 1 (24th March 2021)

Authors:
Mohseni, Marzieh; Babanejad, Mojgan; Booth, Kevin T.; Jamali, Payman; Jalalvand, Khadijeh; Davarnia, Behzad; Ardalani, Fariba; Khoshaeen, Atefeh; Arzhangi, Sanaz; Ghodratpour, Fatemeh; Beheshtian, Maryam; Jahanshad, Faezeh; Otukesh, Hasan; Bahrami, Fatemeh; Seifati, Seyed Morteza; Bazazzadegan, N...
Journal:
Clinical genetics
Issue:
Volume 100:Issue 1(2021)
Page Start:
59
Record Type:
Journal Article
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3. Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of Hearing Loss in Iranian population. Issue 2 (February 2015)

Authors:
Kashef, Atie; Nikzat, Nooshin; Bazzazadegan, Niloofar; Fattahi, Zohreh; Sabbagh-Kermani, Farahnaz; Taghdiri, Maryam; Azadeh, Batool; Mojahedi, Faezeh; Khoshaeen, Atefeh; Habibi, Haleh; Najmabadi, Hossein; Kahrizi, Kimia
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 79:Issue 2(2015:Feb.)
Page Start:
136
Record Type:
Journal Article
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4. G130V de novo mutation in an Iranian pedigree with nonsyndromic hearing loss without palmoplantar keratoderma. (November 2019)

Authors:
Babanejad, Mojgan; Zarandy, Masoud Motasaddi; Nikzat, Nooshin; Bazazzadegan, Niloofar; Arzhangi, Sanaz; Mohseni, Marzieh; Kahrizi, Kimia; Najmabadi, Hossein
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 126(2019:Nov.)
Page Start:
Record Type:
Journal Article
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5. Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss. (February 2019)

Authors:
Mehregan, Hoda; Mohseni, Marzieh; Jalalvand, Khadijeh; Arzhangi, Sanaz; Nikzat, Nooshin; Banihashemi, Sussan; Kahrizi, Kimia; Najmabadi, Hossein
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 117(2019:Feb.)
Page Start:
115
Record Type:
Journal Article
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