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Dastsooz H
12  Ergebnisse:
Personensuche X
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1

Protooncogenic Role of ARHGAP11A and ARHGAP11B in Invasive ..:

Naeimzadeh, Y. ; Ilbeigi, S. ; Dastsooz, H....
BioMed Research International.  2023 (2023)  - p. 1-17 , 2023
Link: https://doi.org/10.1155/..
 
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2

Clinical and molecular characterization of a patient with m..:

Habibzadeh P ; Silawi M ; Dastsooz H...
info:eu-repo/semantics/altIdentifier/pmid/32384880.  , 2020
Link: http://hdl.handle.net/23..
 
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3

Expanding the molecular and clinical phenotypes of FUT8-CDG:

Ng B. G ; Dastsooz H ; Silawi M...
info:eu-repo/semantics/altIdentifier/pmid/32049367.  , 2020
Link: http://hdl.handle.net/23..
 
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4

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

Ziyaee F ; Shorafa E ; Dastsooz H...
info:eu-repo/semantics/altIdentifier/pmid/30642275.  , 2019
Link: http://hdl.handle.net/23..
 
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5

A comprehensive bioinformatics analysis of UBE2C in cancers:

Dastsooz H ; Cereda M ; Donna D.
info:eu-repo/semantics/altIdentifier/pmid/31067633.  , 2019
Link: http://hdl.handle.net/24..
 
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6

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

Habibzadeh P ; Inaloo S ; Silawi M...
info:eu-repo/semantics/altIdentifier/pmid/31551910.  , 2019
Link: http://hdl.handle.net/23..
 
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7

Truncating Mutations in UBAP1 Cause Hereditary Spastic Para..:

Farazi Fard M. A ; Rebelo A. P ; Buglo E...
info:eu-repo/semantics/altIdentifier/pmid/30929741.  , 2019
Link: http://hdl.handle.net/23..
 
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8

Clinical and molecular characterization of three patients w..:

Mahjoub G ; Habibzadeh P ; Dastsooz H...
info:eu-repo/semantics/altIdentifier/pmid/31664948.  , 2019
Link: http://hdl.handle.net/23..
 
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9

A novel frame-shift deletion in FANCF gene causing autosoma..:

Zareifar S ; Dastsooz H ; Shahriari M...
info:eu-repo/semantics/altIdentifier/pmid/31288759.  , 2019
Link: http://hdl.handle.net/23..
 
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10

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

Esmaeilzadeh H ; Bordbar M. R ; Dastsooz H...
info:eu-repo/semantics/altIdentifier/pmid/30029636.  , 2018
Link: http://hdl.handle.net/23..
 
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11

Expanding the molecular and clinical phenotypes of FUT8‐CDG:

Ng, Bobby G. ; Dastsooz, Hassan ; Silawi, Mohammad...
Journal of Inherited Metabolic Disease.  43 (2020)  4 - p. 871-879 , 2020
Link: https://doi.org/10.1002/..
 
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12

Expanding the molecular and clinical phenotypes of FUT8-CDG:

Ng, Bobby G ; Dastsooz, Hassan ; Silawi, Mohammad...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359201/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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