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Amara Fatima

Showing results (1-10 of 9) with videos related to

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Molecular Biotechnology|May 31, 2012
Amplification of GC-rich DNA for high-throughput family-based genetic studiesSadaf Naz, Amara Fatima
Journal of Human Genetics|September 3, 2010
Mutations in CLDN14 are associated with different hearing thresholdsRasheeda Bashir, Amara Fatima, Sadaf Naz
European Journal of Medical Genetics|January 17, 2012
Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing lossRasheeda Bashir, Amara Fatima, Sadaf Naz
Gene|May 24, 2012
A p.C343S missense mutation in PJVK causes progressive hearing lossGhulam Mujtaba, Ihtisham Bukhari, Amara Fatima, et al.
Biochemical Genetics|January 24, 2013
The c.42_52del11 mutation in TPRN and progressive hearing loss in a family from PakistanRasheeda Bashir, Ayesha Imtiaz, Amara Fatima, et al.
European Journal of Medical Genetics|August 21, 2020
A novel homozygous KY variant causing a complex neurological disorderBeenish Arif, Arisha Rasheed, Kishore R Kumar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2011
An unusual neurological syndrome of crawling gait, dystonia, pyramidal signs, and limited speechBeenish Arif, Anne Grünewald, Amara Fatima, et al.
JAMA Neurology|May 24, 2013
A novel OPA3 mutation revealed by exome sequencing: an example of reverse phenotypingBeenish Arif, Kishore R Kumar, Philip Seibler, et al.
Clinical Genetics|August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiersSadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Molecular Biotechnology|May 31, 2012
Amplification of GC-rich DNA for high-throughput family-based genetic studiesSadaf Naz, Amara Fatima
Journal of Human Genetics|September 3, 2010
Mutations in CLDN14 are associated with different hearing thresholdsRasheeda Bashir, Amara Fatima, Sadaf Naz
European Journal of Medical Genetics|January 17, 2012
Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing lossRasheeda Bashir, Amara Fatima, Sadaf Naz
Gene|May 24, 2012
A p.C343S missense mutation in PJVK causes progressive hearing lossGhulam Mujtaba, Ihtisham Bukhari, Amara Fatima, et al.
Biochemical Genetics|January 24, 2013
The c.42_52del11 mutation in TPRN and progressive hearing loss in a family from PakistanRasheeda Bashir, Ayesha Imtiaz, Amara Fatima, et al.
European Journal of Medical Genetics|August 21, 2020
A novel homozygous KY variant causing a complex neurological disorderBeenish Arif, Arisha Rasheed, Kishore R Kumar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2011
An unusual neurological syndrome of crawling gait, dystonia, pyramidal signs, and limited speechBeenish Arif, Anne Grünewald, Amara Fatima, et al.
JAMA Neurology|May 24, 2013
A novel OPA3 mutation revealed by exome sequencing: an example of reverse phenotypingBeenish Arif, Kishore R Kumar, Philip Seibler, et al.
Clinical Genetics|August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiersSadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.
Pageof 1