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Author/Creator Babanejad, Mojgan

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. Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases. Issue 8 (18th June 2019)

Authors:
Najafi, Kimia; Gholami, Soheila; Moshtagh, Azadeh; Bazrgar, Masood; Sadatian, Neda; Abbasi, Golemaryam; Rostami, Parvin; Khalili, Soheila; Babanejad, Mojgan; Nourmohammadi, Bahareh; Faramarzi Garous, Negin; Najmabadi, Hossein; Kariminejad, Roxana
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 8(2019)
Page Start:
n/a
Record Type:
Journal Article
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3. 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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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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6. PDZD7 and hearing loss: More than just a modifier. (29th September 2015)

Authors:
Booth, Kevin T.; Azaiez, Hela; Kahrizi, Kimia; Simpson, Allen C.; Tollefson, William T.A.; Sloan, Christina M.; Meyer, Nicole C.; Babanejad, Mojgan; Ardalani, Fariba; Arzhangi, Sanaz; Schnieders, Michael J.; Najmabadi, Hossein; Smith, Richard J.H.
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 12(2015:Dec.)
Page Start:
2957
Record Type:
Journal Article
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