Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Maryam Rafati

Showing results (1-10 of 31) with videos related to

Pageof 4
Sort By:
Scientific Reports|February 7, 2026
Strategic prioritization for Tehran's electronic waste management via integrated SWOT and QSPM analysisZahra Aliannejadi, Saeed Malmasi, Maryam Rafati
Scientific Reports|October 24, 2025
Modeling environmental noise pollution around the 1893 educational institutions for children in Tehran to support new urban design strategiesNasrin Rigi, Maryam Rafati, Mojgan Zaeimdar, et al.
Human Genetics|March 25, 2009
Novel human pathological mutations. Gene symbol: CDH1. Disease: gastric cancerSaeed Reza Ghaffari, Jila Dastan, Maryam Rafati, et al.
European Journal of Medical Genetics|May 17, 2016
A novel ACVR1 mutation detected by whole exome sequencing in a family with an unusual skeletal dysplasiaMaryam Rafati, Faezeh Mohamadhashem, Azadeh Hoseini, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|July 28, 2011
Her2 amplification status in Iranian breast cancer patients: comparison of immunohistochemistry (IHC) and fluorescence in situ hybridisation (FISH)Saeed Reza Ghaffari, Tayebeh Sabokbar, Jila Dastan, et al.
Clinical Dysmorphology|April 5, 2012
Familial Williams-Beuren syndrome ascertained by screening rather than targeted diagnosisMaryam Rafati, Elaheh Seyyedaboutorabi, Razieh Brujerdi, et al.
BMC Endocrine Disorders|November 5, 2021
Persistent hypercalcemia with similar familial Hypocalciuric hypercalcemia features: a case report and literature reviewMaryam Zahedi, Reyhane Hizomi Arani, Maryam Rafati, et al.
Iranian Journal of Child Neurology|April 8, 2020
Non-progressive Nonimmune Hydrops Fetalis Caused by a Novel Mutation in <i>GUSB</i> GeneAsieh Mosallanejad, Mohammadreza Alaei, Saeed Reza Ghaffari, et al.
Fetal and Pediatric Pathology|April 20, 2016
Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation SequencingMaryam Rafati, Faezeh Mohamadhashem, Azadeh Hoseini, et al.
Journal of Environmental Health Science & Engineering|February 7, 2014
Biochemical responses of juvenile European sturgeon, (Huso huso) to a sub-lethal level of copper and cadmium in freshwater and brackish water environmentsSaeed Zahedi, Arash Akbarzadeh, Maryam Rafati, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Scientific Reports|February 7, 2026
Strategic prioritization for Tehran's electronic waste management via integrated SWOT and QSPM analysisZahra Aliannejadi, Saeed Malmasi, Maryam Rafati
Scientific Reports|October 24, 2025
Modeling environmental noise pollution around the 1893 educational institutions for children in Tehran to support new urban design strategiesNasrin Rigi, Maryam Rafati, Mojgan Zaeimdar, et al.
Human Genetics|March 25, 2009
Novel human pathological mutations. Gene symbol: CDH1. Disease: gastric cancerSaeed Reza Ghaffari, Jila Dastan, Maryam Rafati, et al.
European Journal of Medical Genetics|May 17, 2016
A novel ACVR1 mutation detected by whole exome sequencing in a family with an unusual skeletal dysplasiaMaryam Rafati, Faezeh Mohamadhashem, Azadeh Hoseini, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|July 28, 2011
Her2 amplification status in Iranian breast cancer patients: comparison of immunohistochemistry (IHC) and fluorescence in situ hybridisation (FISH)Saeed Reza Ghaffari, Tayebeh Sabokbar, Jila Dastan, et al.
Clinical Dysmorphology|April 5, 2012
Familial Williams-Beuren syndrome ascertained by screening rather than targeted diagnosisMaryam Rafati, Elaheh Seyyedaboutorabi, Razieh Brujerdi, et al.
BMC Endocrine Disorders|November 5, 2021
Persistent hypercalcemia with similar familial Hypocalciuric hypercalcemia features: a case report and literature reviewMaryam Zahedi, Reyhane Hizomi Arani, Maryam Rafati, et al.
Iranian Journal of Child Neurology|April 8, 2020
Non-progressive Nonimmune Hydrops Fetalis Caused by a Novel Mutation in <i>GUSB</i> GeneAsieh Mosallanejad, Mohammadreza Alaei, Saeed Reza Ghaffari, et al.
Fetal and Pediatric Pathology|April 20, 2016
Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation SequencingMaryam Rafati, Faezeh Mohamadhashem, Azadeh Hoseini, et al.
Journal of Environmental Health Science & Engineering|February 7, 2014
Biochemical responses of juvenile European sturgeon, (Huso huso) to a sub-lethal level of copper and cadmium in freshwater and brackish water environmentsSaeed Zahedi, Arash Akbarzadeh, Maryam Rafati, et al.
Pageof 4