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Yar Muhammad

Showing results (31-40 of 36) with videos related to

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International Journal of Ophthalmology|January 22, 2019
Two novel variants in <i>CYP1B1</i> gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patientsYar Muhammad Waryah, Muhammad Iqbal, Shakeel Ahmed Sheikh, et al.
Molecular Vision|June 28, 2012
Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani familiesMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Journal of Medical Genetics|April 17, 2014
A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular colobomaMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Genes|February 25, 2023
Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani PedigreesAli Raza Rao, Aamir Nazir, Samina Imtiaz, et al.
JPMA. the Journal of the Pakistan Medical Association|October 23, 2021
Clinical Practice Guidelines For The Management Of Colorectal Cancer, A Consensus Statement By The Society Of Surgeons® And Surgical Oncology Society Of Pakistan®Awais Amjad Malik, Muhammad Farooq Afzal, Haroon Javaid Majid, et al.
Plos One|March 17, 2015
Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistanMaleeha Maria, Muhammad Ajmal, Maleeha Azam, et al.
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Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
International Journal of Ophthalmology|January 22, 2019
Two novel variants in <i>CYP1B1</i> gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patientsYar Muhammad Waryah, Muhammad Iqbal, Shakeel Ahmed Sheikh, et al.
Molecular Vision|June 28, 2012
Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani familiesMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Journal of Medical Genetics|April 17, 2014
A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular colobomaMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Genes|February 25, 2023
Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani PedigreesAli Raza Rao, Aamir Nazir, Samina Imtiaz, et al.
JPMA. the Journal of the Pakistan Medical Association|October 23, 2021
Clinical Practice Guidelines For The Management Of Colorectal Cancer, A Consensus Statement By The Society Of Surgeons® And Surgical Oncology Society Of Pakistan®Awais Amjad Malik, Muhammad Farooq Afzal, Haroon Javaid Majid, et al.
Plos One|March 17, 2015
Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistanMaleeha Maria, Muhammad Ajmal, Maleeha Azam, et al.
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