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Maryam Rafati

Showing results (11-20 of 31) with videos related to

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Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|April 13, 2018
Preimplantation High-Resolution HLA Sequencing Using Next Generation SequencingMaryam Rafati, Mohammad Mahdi Akhondi, Mohammad Reza Sadeghi, et al.
The Breast Journal|February 1, 2011
Tracing human papilloma virus in breast tumors of Iranian breast cancer patientsSaeed Reza Ghaffari, Tayebeh Sabokbar, Zahra Meshkat, et al.
Molecular Biology Reports|November 8, 2012
Heterozygosity assessment of five STR loci located at 5q13 region for preimplantation genetic diagnosis of spinal muscular atrophyAsghar Korzebor, Pupak Derakhshandeh-Peykar, Mohsen Meshkani, et al.
Avicenna Journal of Medical Biotechnology|September 6, 2021
Detection of Aneuploidies in Products of Conception and Neonatal Deaths in Iranian Patients Using the Multiplex Ligation-Dependent Probe Amplification (MLPA)Sara Khorami Sarvestani, Maryam Rafati, Haleh Soltanghoraee, et al.
Fetal and Pediatric Pathology|March 24, 2022
Histological Evaluation of Products of Conception, Who Benefits from It?Haleh Soltanghoraee, Arash Mohazzab, Azadeh Soltani, et al.
International Ophthalmology|April 12, 2019
Rhodopsin gene mutation analysis in Iranian patients with autosomal dominant retinitis pigmentosaDanial Roshandel, Maryam Rafati, Sara Khorami, et al.
Molecular Cytogenetics|January 21, 2012
"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangementsMaryam Rafati, Mohammad R Ghadirzadeh, Yaser Heshmati, et al.
Archives of Dermatological Research|December 7, 2023
Whole exome sequencing identifies novel pathogenic variants in TGM1 and ALOX12B in patients with hereditary ichthyosisMitra Chegini, Maryam Eslami, Mahsa Motavaf, et al.
Ophthalmic Genetics|November 18, 2021
Identification of a novel de novo variant in <i>OTX2</i> in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosisMaryam Rafati, Faezeh Mohamadhashem, Koosha Jalilian, et al.
British Journal of Haematology|August 5, 2024
Telomere length and clonal chromosomal alterations in peripheral blood of patients with severe aplastic anaemiaJoshua D Strauss, Derek W Brown, Weiyin Zhou, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|April 13, 2018
Preimplantation High-Resolution HLA Sequencing Using Next Generation SequencingMaryam Rafati, Mohammad Mahdi Akhondi, Mohammad Reza Sadeghi, et al.
The Breast Journal|February 1, 2011
Tracing human papilloma virus in breast tumors of Iranian breast cancer patientsSaeed Reza Ghaffari, Tayebeh Sabokbar, Zahra Meshkat, et al.
Molecular Biology Reports|November 8, 2012
Heterozygosity assessment of five STR loci located at 5q13 region for preimplantation genetic diagnosis of spinal muscular atrophyAsghar Korzebor, Pupak Derakhshandeh-Peykar, Mohsen Meshkani, et al.
Avicenna Journal of Medical Biotechnology|September 6, 2021
Detection of Aneuploidies in Products of Conception and Neonatal Deaths in Iranian Patients Using the Multiplex Ligation-Dependent Probe Amplification (MLPA)Sara Khorami Sarvestani, Maryam Rafati, Haleh Soltanghoraee, et al.
Fetal and Pediatric Pathology|March 24, 2022
Histological Evaluation of Products of Conception, Who Benefits from It?Haleh Soltanghoraee, Arash Mohazzab, Azadeh Soltani, et al.
International Ophthalmology|April 12, 2019
Rhodopsin gene mutation analysis in Iranian patients with autosomal dominant retinitis pigmentosaDanial Roshandel, Maryam Rafati, Sara Khorami, et al.
Molecular Cytogenetics|January 21, 2012
"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangementsMaryam Rafati, Mohammad R Ghadirzadeh, Yaser Heshmati, et al.
Archives of Dermatological Research|December 7, 2023
Whole exome sequencing identifies novel pathogenic variants in TGM1 and ALOX12B in patients with hereditary ichthyosisMitra Chegini, Maryam Eslami, Mahsa Motavaf, et al.
Ophthalmic Genetics|November 18, 2021
Identification of a novel de novo variant in <i>OTX2</i> in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosisMaryam Rafati, Faezeh Mohamadhashem, Koosha Jalilian, et al.
British Journal of Haematology|August 5, 2024
Telomere length and clonal chromosomal alterations in peripheral blood of patients with severe aplastic anaemiaJoshua D Strauss, Derek W Brown, Weiyin Zhou, et al.
Pageof 4