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1 . Academic Journal
Reporting a novel growth hormone receptor gene variant in an Iranian consanguineous pedigree with Laron syndrome: a case report
저자
by
Fatemeh Bitarafan
;
Mehrnoosh Khodaeian
;
Fatemeh Garrousi
;
Raziyeh Khalesi
;
Donya Ghazi Nader
, et al.
소스
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-10 (2023)
Open Access (BioMed Central)
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Web of Science
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7 . Academic Journal
Prevalence and Genotype Distribution of Human Papillomavirus Infection among 12 076 Iranian Women
저자
by
Fatemeh Bitarafan
;
Mohammad Reza Hekmat
;
Mehrnoosh Khodaeian
;
Ehsan Razmara
;
Tahereh Ashrafganjoei
, et al.
소스
International Journal of Infectious Diseases, Vol 111, Iss , Pp 295-302 (2021)
Full Text (ScienceDirect)
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7 . Academic Journal
Novel manifestations of Warburg micro syndrome type 1 caused by a new splicing variant of RAB3GAP1: a case report
저자
by
Raziyeh Khalesi
;
Ehsan Razmara
;
Golareh Asgaritarghi
;
Ali Reza Tavasoli
;
Yasser Riazalhosseini
, et al.
소스
BMC Neurology, Vol 21, Iss 1, Pp 1-13 (2021)
Open Access (BioMed Central)
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7 . Academic Journal
Investigation of Inherited Causes of Autosomal Recessive Non-syndromic Epilepsy in an Iranian Family Using Whole Exome Sequencing Method
저자
by
Raziyeh Khalesi
;
Masoud Garshasbi
;
Mahmood Tavallaei
.
소스
مجله دانشکده پزشکی اصفهان, Vol 34, Iss 407, Pp 1362-1368 (2017)
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Find it @ DONGA
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5 .
Identification of a Novel Splice Site Mutation in RUNX2 Gene in a Family with Rare Autosomal Dominant Cleidocranial Dysplasia
저자
by
Raziyeh Khalesi
;
Masoud Garshasbi
;
Fatemeh Bitarafan
;
Ebrahim Jamali
;
Navid Almadani
.
소스
Iranian Biomedical Journal
Open Access (OpenAIRE)
Scopus
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7 .
Pathogenic DST sequence variants result in either epidermolysis bullosa simplex (EBS) or hereditary sensory and autonomic neuropathy type 6 (HSAN-VI)
저자
by
Raziyeh Khalesi
;
Nailah Harvey
;
Masoud Garshasbi
;
Elnaz Kalamati
;
Leila Youssefian
, et al.
소스
Experimental dermatologyREFERENCES
. 31(6)
Full Text (Wiley)
Scopus
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7 .
Prevalence and Genotype Distribution of Human Papillomavirus Infection among 12 076 Iranian Women
저자
by
Mohammad Reza Hekmat
;
Mitra Modares Gilani
;
Raziyeh Khalesi
;
Tahereh Ashrafganjoei
;
Soheila Sarmadi
, et al.
소스
International Journal of Infectious Diseases, Vol 111, Iss, Pp 295-302 (2021)
Open Access (OpenAIRE)
JCR 저널정보
요약보기
Export
E-Mail
EndNote
RefWorks
7 .
Novel manifestations of Warburg micro syndrome type 1 caused by a new splicing variant of RAB3GAP1: a case report
저자
by
Ali Reza Tavasoli
;
Golareh Asgaritarghi
;
Yasser Riazalhosseini
;
Ehsan Razmara
;
Masoud Garshasbi
, et al.
소스
BMC Neurology, Vol 21, Iss 1, Pp 1-13 (2021)
BMC Neurology
Open Access (BioMed Central)
Open Access (OpenAIRE)
Scopus
JCR 저널정보
요약보기
Export
E-Mail
EndNote
RefWorks
7 .
Identification of Novel Mutation in EIF2AK3 Gene as a Causal Variant in a Family With Rare Disease
저자
by
Raziyeh Khalesi
;
Masoud Garshasbi
.
소스
Journal of Medical Cases
. 8:102-104
Open Access (OpenAIRE)
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4 .
Propionic Academia: Exome Sequencing Identified Novel Mutation in Exon 12 of PCCA Gene
저자
by
Raziyeh Khalesi
;
Masoud Garshasbi
.
소스
Journal of Medical Cases
. 8:111-113
Open Access (OpenAIRE)
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