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Babanejad, Mojgan
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1

P604: Diagnostic utility of NGS testing in a highly consang..:

Abolhassani, Ayda ; Fattahi, Zohreh ; Beheshtian, Maryam...
Genetics in Medicine Open.  2 (2024)  - p. 101510 , 2024
Link: https://doi.org/10.1016/..
 
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2

Clinical application of next generation sequencing for Mend..:

Abolhassani, Ayda ; Fattahi, Zohreh ; Beheshtian, Maryam...
npj Genomic Medicine.  9 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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3

Identification of a homozygous frameshift mutation in the F..:

Jamshidi, Fereshteh ; Shokouhian, Ebrahim ; Mohseni, Marzieh...
Molecular Genetics & Genomic Medicine.  11 (2023)  5 - p. , 2023
Link: https://doi.org/10.1002/..
 
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4

Genetic etiology of hearing loss in Iran:

Babanejad, Mojgan ; Beheshtian, Maryam ; Jamshidi, Fereshteh...
Human Genetics.  , 2022
Link: https://doi.org/10.1007/..
 
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5

Exome sequencing utility in defining the genetic landscape ..:

Mohseni, Marzieh ; Babanejad, Mojgan ; Booth, Kevin T....
Clinical Genetics.  100 (2021)  1 - p. 59-78 , 2021
Link: https://doi.org/10.1111/..
 
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6

When transcripts matter: delineating between non-syndromic ..:

Mohseni, Marzieh ; Akbari, Mojdeh ; Booth, Kevin T....
Journal of Human Genetics.  65 (2020)  7 - p. 609-617 , 2020
Link: https://doi.org/10.1038/..
 
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7

Chromosomal aberrations in pregnancy and fetal loss: Insigh..:

Najafi, Kimia ; Gholami, Soheila ; Moshtagh, Azadeh...
Molecular Genetics & Genomic Medicine.  7 (2019)  8 - p. , 2019
Link: https://doi.org/10.1002/..
 
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8

G130V de novo mutation in an Iranian pedigree with nonsyndr..:

Babanejad, Mojgan ; Zarandy, Masoud Motasaddi ; Nikzat, Nooshin...
International Journal of Pediatric Otorhinolaryngology.  126 (2019)  - p. 109607 , 2019
Link: https://doi.org/10.1016/..
 
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9

SLC52A2 mutations cause SCABD2 phenotype: A second report:

Babanejad, Mojgan ; Adeli, Omid Ali ; Nikzat, Nooshin...
International Journal of Pediatric Otorhinolaryngology.  104 (2018)  - p. 195-199 , 2018
Link: https://doi.org/10.1016/..
 
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10

C-reactive protein and complement factor H polymorphism int..:

Soheilian, Roham ; Jabbarpour Bonyadi, Mohammad Hossein ; Moein, Hamidreza...
International Ophthalmology.  37 (2016)  5 - p. 1161-1168 , 2016
Link: https://doi.org/10.1007/..
 
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11

PDZD7 and hearing loss: More than just a modifier:

Booth, Kevin T. ; Azaiez, Hela ; Kahrizi, Kimia...
American Journal of Medical Genetics Part A.  167 (2015)  12 - p. 2957-2965 , 2015
Link: https://doi.org/10.1002/..
 
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12

Two novel mutations in ILDR1 gene cause autosomal recessive..:

MEHRJOO, ZOHREH ; BABANEJAD, MOJGAN ; KAHRIZI, KIMIA.
Journal of Genetics.  94 (2015)  3 - p. 483-487 , 2015
Link: https://doi.org/10.1007/..
 
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13

Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri pat..:

Davarnia, Behzad ; Babanejad, Mojgan ; Fattahi, Zohreh...
International Journal of Pediatric Otorhinolaryngology.  76 (2012)  2 - p. 268-271 , 2012
Link: https://doi.org/10.1016/..
 
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14

Screening for MYO15A gene mutations in autosomal recessive ..:

Fattahi, Zohreh ; Shearer, A. Eliot ; Babanejad, Mojgan...
American Journal of Medical Genetics Part A.  158A (2012)  8 - p. 1857-1864 , 2012
Link: https://doi.org/10.1002/..
 
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15

The spectrum of GJB2 mutations in the Iranian population wi..:

Bazazzadegan, Niloofar ; Nikzat, Nooshin ; Fattahi, Zohreh...
International Journal of Pediatric Otorhinolaryngology.  76 (2012)  8 - p. 1164-1174 , 2012
Link: https://doi.org/10.1016/..
 
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