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The International Journal of Pharmacy Practice
|
February 20, 2026
Diversity, equality, and inclusivity in pharmacy services: a scoping review
Umm-E- Kalsoom, Amjad Khan, Sara Garfield
Pediatrics International : Official Journal of the Japan Pediatric Society
|
September 12, 2009
A novel missense mutation in the EVC gene underlies Ellis-van Creveld syndrome in a Pakistani family
Umm-E-Kalsoom, Naveed Wasif, Muhammad Tariq, et al.
JPMA. the Journal of the Pakistan Medical Association
|
September 26, 2014
Malignant transformations in ovarian teratomas: a report of four cases
Abdul Hannan, Umm-e-Kalsoom Awan, Neelam Siddiqui, et al.
Genetic Testing and Molecular Biomarkers
|
March 29, 2020
A Novel Missense Variant in the <i>ALX4</i> Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous Family
Shabir Hussain, Umm-E-Kalsoom, Irfan Ullah, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
February 7, 2026
The role of NADPH oxidases in central nervous system regulation of hypertension: Mechanisms and therapeutic insights
Umm-E Kalsoom, Jing Jin, Wanying Meng, et al.
Journal of Human Genetics
|
December 8, 2017
Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny
Asmat Ullah, Muhammad Umair, Umm E-Kalsoom, et al.
International Journal of Clinical Pharmacy
|
November 14, 2025
Estimation of carbon emissions from inhaled respiratory medicines in Ireland: a cross-sectional study from a national pharmacy claims database from 2020 to 2022
Hafsa Kanwal, Umm-E-Kalsoom, Amjad Khan, et al.
Anais Brasileiros De Dermatologia
|
May 14, 2023
A novel homozygous nonsense mutation in NECTIN4 gene in a Pakistani family with ectodermal dysplasia syndactyly syndrome 1
Bibi Hajra, Abdullah, Nousheen Bibi, et al.
Primary Care Diabetes
|
July 4, 2015
Evaluation of diabetes awareness among general population of Bahawalpur, Pakistan
Imran Masood, Ahsan Saleem, Asma Hassan, et al.
Human Genetics
|
August 31, 2011
Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3-q21.2 and screening of the candidate genes
Umm-e-Kalsoom, Sulman Basit, Syed Kamran-ul-Hassan Naqvi, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
The International Journal of Pharmacy Practice
|
February 20, 2026
Diversity, equality, and inclusivity in pharmacy services: a scoping review
Umm-E- Kalsoom, Amjad Khan, Sara Garfield
Pediatrics International : Official Journal of the Japan Pediatric Society
|
September 12, 2009
A novel missense mutation in the EVC gene underlies Ellis-van Creveld syndrome in a Pakistani family
Umm-E-Kalsoom, Naveed Wasif, Muhammad Tariq, et al.
JPMA. the Journal of the Pakistan Medical Association
|
September 26, 2014
Malignant transformations in ovarian teratomas: a report of four cases
Abdul Hannan, Umm-e-Kalsoom Awan, Neelam Siddiqui, et al.
Genetic Testing and Molecular Biomarkers
|
March 29, 2020
A Novel Missense Variant in the <i>ALX4</i> Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous Family
Shabir Hussain, Umm-E-Kalsoom, Irfan Ullah, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
February 7, 2026
The role of NADPH oxidases in central nervous system regulation of hypertension: Mechanisms and therapeutic insights
Umm-E Kalsoom, Jing Jin, Wanying Meng, et al.
Journal of Human Genetics
|
December 8, 2017
Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny
Asmat Ullah, Muhammad Umair, Umm E-Kalsoom, et al.
International Journal of Clinical Pharmacy
|
November 14, 2025
Estimation of carbon emissions from inhaled respiratory medicines in Ireland: a cross-sectional study from a national pharmacy claims database from 2020 to 2022
Hafsa Kanwal, Umm-E-Kalsoom, Amjad Khan, et al.
Anais Brasileiros De Dermatologia
|
May 14, 2023
A novel homozygous nonsense mutation in NECTIN4 gene in a Pakistani family with ectodermal dysplasia syndactyly syndrome 1
Bibi Hajra, Abdullah, Nousheen Bibi, et al.
Primary Care Diabetes
|
July 4, 2015
Evaluation of diabetes awareness among general population of Bahawalpur, Pakistan
Imran Masood, Ahsan Saleem, Asma Hassan, et al.
Human Genetics
|
August 31, 2011
Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3-q21.2 and screening of the candidate genes
Umm-e-Kalsoom, Sulman Basit, Syed Kamran-ul-Hassan Naqvi, et al.
Page
of 4