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Tahir Naeem

Showing results (11-20 of 26) with videos related to

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Saudi Medical Journal|July 17, 2014
Changing epidemiology of tuberculosis detected by an 8-year retrospective laboratory study in a tertiary teaching hospital in central Saudi ArabiaAli M Somily, Tahir Naeem, Hanan A Habib, et al.
BMC Medical Genetics|June 26, 2014
Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophyJens Schuster, Tahir Naeem Khan, Muhammad Tariq, et al.
BMC Medical Genetics|December 14, 2012
Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I)Tahir Naeem Khan, Joakim Klar, Sadia Nawaz, et al.
European Journal of Human Genetics : EJHG|January 30, 2014
Evidence for autosomal recessive inheritance in SPG3A caused by homozygosity for a novel ATL1 missense mutationTahir Naeem Khan, Joakim Klar, Muhammad Tariq, et al.
Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society|August 21, 2013
Value of microbiology study in congenital nasolacrimal duct obstructionYasser H Al-Faky, Tahir Naeem, Nora Al-Sobaie, et al.
Plos One|April 10, 2014
Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosisDoroteya Raykova, Joakim Klar, Aysha Azhar, et al.
Journal of Medical Genetics|July 5, 2015
Whole exome sequencing identifies LRP1 as a pathogenic gene in autosomal recessive keratosis pilaris atrophicansJoakim Klar, Jens Schuster, Tahir Naeem Khan, et al.
BMC Medical Genomics|November 10, 2021
Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variantsChunyu Liu, Muhammad Ajmal, Zaineb Akram, et al.
BMC Medical Genetics|December 16, 2014
A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiencyMuhammad Jameel, Joakim Klar, Muhammad Tariq, et al.
JMIR Medical Informatics|March 24, 2026
A Bilingual Arabic-English Ambient AI Scribe for Clinical Documentation: Prospective Evaluation StudyUmair Tahir Khan, Ammar Tahir Khan, Waleed Aljaadi, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Saudi Medical Journal|July 17, 2014
Changing epidemiology of tuberculosis detected by an 8-year retrospective laboratory study in a tertiary teaching hospital in central Saudi ArabiaAli M Somily, Tahir Naeem, Hanan A Habib, et al.
BMC Medical Genetics|June 26, 2014
Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophyJens Schuster, Tahir Naeem Khan, Muhammad Tariq, et al.
BMC Medical Genetics|December 14, 2012
Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I)Tahir Naeem Khan, Joakim Klar, Sadia Nawaz, et al.
European Journal of Human Genetics : EJHG|January 30, 2014
Evidence for autosomal recessive inheritance in SPG3A caused by homozygosity for a novel ATL1 missense mutationTahir Naeem Khan, Joakim Klar, Muhammad Tariq, et al.
Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society|August 21, 2013
Value of microbiology study in congenital nasolacrimal duct obstructionYasser H Al-Faky, Tahir Naeem, Nora Al-Sobaie, et al.
Plos One|April 10, 2014
Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosisDoroteya Raykova, Joakim Klar, Aysha Azhar, et al.
Journal of Medical Genetics|July 5, 2015
Whole exome sequencing identifies LRP1 as a pathogenic gene in autosomal recessive keratosis pilaris atrophicansJoakim Klar, Jens Schuster, Tahir Naeem Khan, et al.
BMC Medical Genomics|November 10, 2021
Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variantsChunyu Liu, Muhammad Ajmal, Zaineb Akram, et al.
BMC Medical Genetics|December 16, 2014
A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiencyMuhammad Jameel, Joakim Klar, Muhammad Tariq, et al.
JMIR Medical Informatics|March 24, 2026
A Bilingual Arabic-English Ambient AI Scribe for Clinical Documentation: Prospective Evaluation StudyUmair Tahir Khan, Ammar Tahir Khan, Waleed Aljaadi, et al.
Pageof 3