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Muhammad Ansar

Showing results (111-120 of 191) with videos related to

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Human Genome Variation|April 27, 2026
Duplication of 4-bp in SACS leads to autosomal recessive spastic ataxia of Charlevoix-Saguenay type in two Pakistani patientsSaba Bibi, Asad Munir, Fawad Ali, et al.
Human Molecular Genetics|March 11, 2021
Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2Stylianos E Antonarakis, Aleš Holoubek, Melivoia Rapti, et al.
Environmental Science and Pollution Research International|March 29, 2021
Compact maize canopy improves radiation use efficiency and grain yield of maize/soybean relay intercropping systemMuhammad Ali Raza, Liang Cui, Imran Khan, et al.
Scientific Reports|March 22, 2019
Effect of planting patterns on yield, nutrient accumulation and distribution in maize and soybean under relay intercropping systemsMuhammad Ali Raza, Muhammad Hayder Bin Khalid, Xia Zhang, et al.
Neurogenetics|May 5, 2006
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: Novel sequence variants in ASPM geneAsma Gul, Muhammad Jawad Hassan, Saqib Mahmood, et al.
Human Genetics|November 2, 2005
A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3Muhammad Jawad Hassan, Regie Lyn P Santos, Muhammad Arshad Rafiq, et al.
Human Molecular Genetics|March 5, 2020
Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short statureMuhammad Ansar, Frédéric Ebstein, Hayriye Özkoç, et al.
European Journal of Human Genetics : EJHG|October 11, 2023
A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndromeMadiha Amin Malik, Muhammad Arif Nadeem Saqib, Edwin Mientjes, et al.
Human Mutation|September 1, 2005
Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairmentRegie Lyn P Santos, Muhammad Wajid, Mohammad Nasim Khan, et al.
Journal of Medical Genetics|July 11, 2015
A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hairMuhammad Ansar, Syed Irfan Raza, Kwanghyuk Lee, et al.
Pageof 20

Showing results (111-120 of 191) with videos related to

Sort By:
Pageof 20
Human Genome Variation|April 27, 2026
Duplication of 4-bp in SACS leads to autosomal recessive spastic ataxia of Charlevoix-Saguenay type in two Pakistani patientsSaba Bibi, Asad Munir, Fawad Ali, et al.
Human Molecular Genetics|March 11, 2021
Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2Stylianos E Antonarakis, Aleš Holoubek, Melivoia Rapti, et al.
Environmental Science and Pollution Research International|March 29, 2021
Compact maize canopy improves radiation use efficiency and grain yield of maize/soybean relay intercropping systemMuhammad Ali Raza, Liang Cui, Imran Khan, et al.
Scientific Reports|March 22, 2019
Effect of planting patterns on yield, nutrient accumulation and distribution in maize and soybean under relay intercropping systemsMuhammad Ali Raza, Muhammad Hayder Bin Khalid, Xia Zhang, et al.
Neurogenetics|May 5, 2006
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: Novel sequence variants in ASPM geneAsma Gul, Muhammad Jawad Hassan, Saqib Mahmood, et al.
Human Genetics|November 2, 2005
A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3Muhammad Jawad Hassan, Regie Lyn P Santos, Muhammad Arshad Rafiq, et al.
Human Molecular Genetics|March 5, 2020
Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short statureMuhammad Ansar, Frédéric Ebstein, Hayriye Özkoç, et al.
European Journal of Human Genetics : EJHG|October 11, 2023
A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndromeMadiha Amin Malik, Muhammad Arif Nadeem Saqib, Edwin Mientjes, et al.
Human Mutation|September 1, 2005
Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairmentRegie Lyn P Santos, Muhammad Wajid, Mohammad Nasim Khan, et al.
Journal of Medical Genetics|July 11, 2015
A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hairMuhammad Ansar, Syed Irfan Raza, Kwanghyuk Lee, et al.
Pageof 20