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Sherin Shaaban

Showing results (1-10 of 23) with videos related to

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The Journal of Applied Laboratory Medicine|January 3, 2024
Interrogating Pharmacogenetics Using Next-Generation SequencingYuan Ji, Sherin Shaaban
Frontiers in Genetics|February 9, 2023
Pharmacogenomics and health disparities, are we helping?Sherin Shaaban, Yuan Ji
Molecular Vision|July 15, 2009
Investigation of parent-of-origin effect in comitant strabismus using MOD score analysisSherin Shaaban, Toshihiko Matsuo, Konstantin Strauch, et al.
Pharmacogenomics|February 17, 2025
<i>TPMT</i> and <i>NUDT15</i> genotyping, TPMT enzyme activity and metabolite determination for thiopurines therapy: a reference laboratory experienceSherin Shaaban, Brandon S Walker, Yuan Ji, et al.
Middle East African Journal of Ophthalmology|February 10, 2010
Low vision AIDS provision for visually impaired egyptian patients - a clinical outcomeSherin Shaaban, Ahmad Rashid El-Lakkany, Ashraf Swelam, et al.
The Journal of Molecular Diagnostics : JMD|October 2, 2024
A Single Multiplex PCR and Single-Nucleotide Extension Assay for the Detection of Common Thanatophoric Dysplasia I and II MutationsMohamed A Jama, N Scott Reading, Eric Fredrickson, et al.
Journal of Human Reproductive Sciences|July 12, 2019
Genetics of Female Infertility: Molecular Study of Newborn Ovary Homeobox Gene in Poor Ovarian RespondersOsamah Batiha, Nour Alhoda Alahmad, Amer Sindiani, et al.
Investigative Ophthalmology & Visual Science|October 1, 2008
Chromosomes 4q28.3 and 7q31.2 as new susceptibility loci for comitant strabismusSherin Shaaban, Toshihiko Matsuo, Hirotake Fujiwara, et al.
Investigative Ophthalmology & Visual Science|July 1, 2011
Expansion of the CHN1 strabismus phenotypeNoriko Miyake, Joseph L Demer, Sherin Shaaban, et al.
JAMA Ophthalmology|October 5, 2013
RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermiaSherin Shaaban, Leigh Ramos-Platt, Floyd H Gilles, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
The Journal of Applied Laboratory Medicine|January 3, 2024
Interrogating Pharmacogenetics Using Next-Generation SequencingYuan Ji, Sherin Shaaban
Frontiers in Genetics|February 9, 2023
Pharmacogenomics and health disparities, are we helping?Sherin Shaaban, Yuan Ji
Molecular Vision|July 15, 2009
Investigation of parent-of-origin effect in comitant strabismus using MOD score analysisSherin Shaaban, Toshihiko Matsuo, Konstantin Strauch, et al.
Pharmacogenomics|February 17, 2025
<i>TPMT</i> and <i>NUDT15</i> genotyping, TPMT enzyme activity and metabolite determination for thiopurines therapy: a reference laboratory experienceSherin Shaaban, Brandon S Walker, Yuan Ji, et al.
Middle East African Journal of Ophthalmology|February 10, 2010
Low vision AIDS provision for visually impaired egyptian patients - a clinical outcomeSherin Shaaban, Ahmad Rashid El-Lakkany, Ashraf Swelam, et al.
The Journal of Molecular Diagnostics : JMD|October 2, 2024
A Single Multiplex PCR and Single-Nucleotide Extension Assay for the Detection of Common Thanatophoric Dysplasia I and II MutationsMohamed A Jama, N Scott Reading, Eric Fredrickson, et al.
Journal of Human Reproductive Sciences|July 12, 2019
Genetics of Female Infertility: Molecular Study of Newborn Ovary Homeobox Gene in Poor Ovarian RespondersOsamah Batiha, Nour Alhoda Alahmad, Amer Sindiani, et al.
Investigative Ophthalmology & Visual Science|October 1, 2008
Chromosomes 4q28.3 and 7q31.2 as new susceptibility loci for comitant strabismusSherin Shaaban, Toshihiko Matsuo, Hirotake Fujiwara, et al.
Investigative Ophthalmology & Visual Science|July 1, 2011
Expansion of the CHN1 strabismus phenotypeNoriko Miyake, Joseph L Demer, Sherin Shaaban, et al.
JAMA Ophthalmology|October 5, 2013
RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermiaSherin Shaaban, Leigh Ramos-Platt, Floyd H Gilles, et al.
Pageof 3