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Umm-E-Kalsoom

Showing results (31-40 of 38) with videos related to

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European Journal of Dermatology : EJD|August 22, 2020
Homozygous variants of EDAR underlying hypohidrotic ectodermal dysplasia in three consanguineous familiesSher Alam Khan, Ayesha Rukan, Asmat Ullah, et al.
Frontiers in Genetics|February 11, 2022
The First Report of a Missense Variant in <i>RFX2</i> Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani FamilySher Alam Khan, Saadullah Khan, Noor Muhammad, et al.
Klinische Padiatrie|September 20, 2021
Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous FamiliesWarda Nawal, Asmat Ullah, Ubaid Ullah, et al.
Genes|September 27, 2025
Novel <i>KIAA0825</i> Variants Underlie Nonsyndromic Postaxial PolydactylyAbdullah, Thashi Bharadwaj, Saffia Javed, et al.
Human Genetics|December 25, 2010
DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2Sulman Basit, Kwanghyuk Lee, Rabia Habib, et al.
ACS Applied Bio Materials|January 11, 2022
Antidiabetic and Hypolipidemic Potential of Green AgNPs against Diabetic MiceSalim Ullah, Syed Wadud Ali Shah, Muhammad Tauseef Qureshi, et al.
Genetic Testing and Molecular Biomarkers|August 9, 2020
Sequence Variants in the <i>WNT10B</i> and <i>TP63</i> Genes Underlying Isolated Split-Hand/Split-Foot MalformationMuhammad Bilal, Amir Hayat, Muhammad Umair, et al.
Clinical and Experimental Dermatology|March 24, 2011
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from PakistanS Khan, R Habib, H Mir, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
European Journal of Dermatology : EJD|August 22, 2020
Homozygous variants of EDAR underlying hypohidrotic ectodermal dysplasia in three consanguineous familiesSher Alam Khan, Ayesha Rukan, Asmat Ullah, et al.
Frontiers in Genetics|February 11, 2022
The First Report of a Missense Variant in <i>RFX2</i> Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani FamilySher Alam Khan, Saadullah Khan, Noor Muhammad, et al.
Klinische Padiatrie|September 20, 2021
Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous FamiliesWarda Nawal, Asmat Ullah, Ubaid Ullah, et al.
Genes|September 27, 2025
Novel <i>KIAA0825</i> Variants Underlie Nonsyndromic Postaxial PolydactylyAbdullah, Thashi Bharadwaj, Saffia Javed, et al.
Human Genetics|December 25, 2010
DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2Sulman Basit, Kwanghyuk Lee, Rabia Habib, et al.
ACS Applied Bio Materials|January 11, 2022
Antidiabetic and Hypolipidemic Potential of Green AgNPs against Diabetic MiceSalim Ullah, Syed Wadud Ali Shah, Muhammad Tauseef Qureshi, et al.
Genetic Testing and Molecular Biomarkers|August 9, 2020
Sequence Variants in the <i>WNT10B</i> and <i>TP63</i> Genes Underlying Isolated Split-Hand/Split-Foot MalformationMuhammad Bilal, Amir Hayat, Muhammad Umair, et al.
Clinical and Experimental Dermatology|March 24, 2011
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from PakistanS Khan, R Habib, H Mir, et al.
Pageof 4