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Fard, Mohammad Ali Farazi
31  results:
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1

A novel splice site mutation in WAS gene in patient with Wi..:

Esmaeilzadeh, Hossein ; Bordbar, Mohammad Reza ; Dastsooz, Hassan...
BMC Medical Genetics.  19 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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2

Novel mutations in PANK2 and PLA2G6 genes in patients with ..:

Dastsooz, Hassan ; Nemati, Hamid ; Fard, Mohammad Ali Farazi..
BMC Medical Genetics.  18 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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3

Biallelic variants in TMEM222 cause a new autosomal recessi..:

Polla, Daniel L. ; Farazi Fard, Mohammad Ali ; Tabatabaei, Zahra...
Genetics in Medicine.  23 (2021)  7 - p. 1246-1254 , 2021
Link: https://doi.org/10.1038/..
 
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4

Identification of novel microsatellite markers flanking GJB..:

Tabatabaei, Zahra ; Farazi Fard, Mohammad Ali ; Hashemi, Seyed Basir.
European Journal of Medical Genetics.  63 (2020)  4 - p. 103796 , 2020
Link: https://doi.org/10.1016/..
 
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5

Pre-implantation genetic diagnosis in an Iranian family wit..:

Habibzadeh, Parham ; Tabatabaei, Zahra ; Farazi Fard, Mohammad Ali...
BMC Medical Genetics.  21 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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6

A novel mutation in SEPN1 causing rigid spine muscular dyst..:

Ziyaee, Fateme ; Shorafa, Eslam ; Dastsooz, Hassan...
BMC Medical Genetics.  20 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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7

A Novel TTC19 Mutation in a Patient With Neurological, Psyc..:

Habibzadeh, Parham ; Inaloo, Soroor ; Silawi, Mohammad...
Frontiers in Neurology.  10 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
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8

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome:

Taghdiri, Maryam ; Dastsooz, Hassan ; Fardaei, Majid...
Frontiers in Pediatrics.  5 (2017)  - p. , 2017
Link: https://doi.org/10.3389/..
 
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9

A case report of novel mutation in PRF1 gene, which causes ..:

Bordbar, Mohammad Reza ; Modarresi, Farzaneh ; Farazi Fard, Mohammad Ali...
BMC Medical Genetics.  18 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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10

Biallelic variants in TMEM222 cause a new autosomal recessi..:

Polla, Daniel L ; Fard, Mohammad Ali Farazi ; Tabatabaei, Zahra...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725574/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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11

Prenatal diagnosis of Sex determining region Y -box transcr..:

Pooneh Nikuei ; Ph.D ; Zahra Khashavy...
https://doi.org/10.18502/ijrm.v21i8.14022.  , 2023
Link: https://doi.org/10.18502..
 
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12

Pre-Implantation Genetic Testing for Monogenic Disorders (P..:

Zahra Tabatabaei ; Khadijeh Karbalaie ; Parham Habibzadeh...
https://celljournal.org/journal/article/fulltext/pre-implantation-genetic-diagnosis-in-a-family-with-a-novel-mutation-in-dpagt1-gene.pdf.  , 2021
Link: https://doi.org/10.22074..
 
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13

Pre-implantation genetic diagnosis in an Iranian family wit..:

Parham Habibzadeh ; Zahra Tabatabaei ; Mohammad Ali Farazi Fard...
https://doi.org/10.1186/s12881-020-0959-8.  , 2020
Link: https://doi.org/10.1186/..
 
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14

A Novel TTC19 Mutation in a Patient With Neurological, Psyc..:

Parham Habibzadeh ; Soroor Inaloo ; Mohammad Silawi...
https://www.frontiersin.org/article/10.3389/fneur.2019.00944/full.  , 2019
Link: https://doi.org/10.3389/..
 
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15

Truncating Mutations in UBAP1 Cause Hereditary Spastic Para..:

Farazi Fard, Mohammad Ali ; Rebelo, Adriana P ; Buglo, Elena...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557723/.  , 2019
Link: http://www.ncbi.nlm.nih...
 
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