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Rasheeda Bashir

Showing results (21-30 of 27) with videos related to

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Veterinary Research Forum : an International Quarterly Journal|February 2, 2026
Comparative analysis of VP1 epitopic variation among different isolates of foot-and-mouth disease virus type-O during an outbreak in the Punjab province of PakistanAtia Rasheed, Imran Altaf, Faisal Ayub, et al.
Genes|February 25, 2023
Exome Sequencing Reveals <i>SLC4A11</i> Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital GlaucomaKhazeema Yousaf, Sadaf Naz, Asma Mushtaq, et al.
Molecular Biology Reports|January 15, 2024
Investigating the effects of a single ASPM variant (c.8508_8509) on brain architecture among siblings in a consanguineous Pakistani familyKomal Aslam, Aysha Saeed, Iffat Jamil, et al.
Molecular Biology Reports|June 26, 2024
Molecular genetics, neuroimaging outcomes, and structural analyses of novel and recurrent variants of WDR62 gene in two consanguineous Pakistani families with autosomal recessive primary microcephalyKomal Aslam, Aysha Saeed, Hafiza Iqra Saeed, 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.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
Human Molecular Genetics|January 3, 2018
CDC14A phosphatase is essential for hearing and male fertility in mouse and humanAyesha Imtiaz, Inna A Belyantseva, Alisha J Beirl, et al.
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Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Veterinary Research Forum : an International Quarterly Journal|February 2, 2026
Comparative analysis of VP1 epitopic variation among different isolates of foot-and-mouth disease virus type-O during an outbreak in the Punjab province of PakistanAtia Rasheed, Imran Altaf, Faisal Ayub, et al.
Genes|February 25, 2023
Exome Sequencing Reveals <i>SLC4A11</i> Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital GlaucomaKhazeema Yousaf, Sadaf Naz, Asma Mushtaq, et al.
Molecular Biology Reports|January 15, 2024
Investigating the effects of a single ASPM variant (c.8508_8509) on brain architecture among siblings in a consanguineous Pakistani familyKomal Aslam, Aysha Saeed, Iffat Jamil, et al.
Molecular Biology Reports|June 26, 2024
Molecular genetics, neuroimaging outcomes, and structural analyses of novel and recurrent variants of WDR62 gene in two consanguineous Pakistani families with autosomal recessive primary microcephalyKomal Aslam, Aysha Saeed, Hafiza Iqra Saeed, 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.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
Human Molecular Genetics|January 3, 2018
CDC14A phosphatase is essential for hearing and male fertility in mouse and humanAyesha Imtiaz, Inna A Belyantseva, Alisha J Beirl, et al.
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