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Showing results (831-840 of 1,167) with videos related to
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The Journal of Gene Medicine
|
January 25, 2022
Homozygous missense variant in POPDC3 causes recessive limb-girdle muscular dystrophy type 26
Anwar Ullah, Zhaohan Lin, Muhammad Younus, et al.
Pediatric Research
|
July 1, 2017
Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3
Muhammad Umair, Bader Alhaddad, Afzal Rafique, et al.
Materials (Basel, Switzerland)
|
November 11, 2022
Prediction of Autogenous Shrinkage of Concrete Incorporating Super Absorbent Polymer and Waste Materials through Individual and Ensemble Machine Learning Approaches
Hisham Jahangir Qureshi, Muhammad Umair Saleem, Muhammad Faisal Javed, et al.
Transplantation and Cellular Therapy
|
January 4, 2025
Outcomes of Allogeneic Hematopoietic Stem Cell Transplantation in Patients Aged 70 Years and Older: A Systematic Review and Meta-Analysis
Moazzam Shahzad, Qamar Iqbal, Muhammad Kashif Amin, et al.
Academic Radiology
|
February 1, 2025
Cardiac Amyloidosis: A Comprehensive Review of Imaging Findings
Alireza Mohseni, Ghazal Zandieh, Kristin Porter, et al.
BMC Plant Biology
|
July 26, 2024
Multiple cropping effectively increases soil bacterial diversity, community abundance and soil fertility of paddy fields
Haiying Tang, Ying Liu, Xiaoqi Yang, et al.
Ticks and Tick-Borne Diseases
|
April 30, 2023
First molecular confirmation of multiple zoonotic vector-borne diseases in pet dogs and cats of Hong Kong SAR
Sabir Hussain, Abrar Hussain, Muhammad Umair Aziz, et al.
Sensors (Basel, Switzerland)
|
April 12, 2022
Modeling of Efficient Control Strategies for LCC-HVDC Systems: A Case Study of Matiari-Lahore HVDC Power Transmission Line
Adeel Ahmed, Danish Khan, Ahmed Muddassir Khan, et al.
Frontiers in Pediatrics
|
September 27, 2019
Biallelic Missense Mutation in the <i>ECEL1</i> Underlies Distal Arthrogryposis Type 5 (DA5D)
Muhammad Umair, Amjad Khan, Amir Hayat, et al.
Molecular Syndromology
|
April 3, 2025
A Novel Loss of Function Variant in <i>HCN1</i> Gene Underlies Early Infantile Epileptic Encephalopathy 24 [EIEE24]
Mujahid, Ahmed Waqas, Ibrahim A Almazni, et al.
Page
of 117
Search research articles
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Showing results (831-840 of 1,167) with videos related to
Sort By:
Page
of 117
The Journal of Gene Medicine
|
January 25, 2022
Homozygous missense variant in POPDC3 causes recessive limb-girdle muscular dystrophy type 26
Anwar Ullah, Zhaohan Lin, Muhammad Younus, et al.
Pediatric Research
|
July 1, 2017
Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3
Muhammad Umair, Bader Alhaddad, Afzal Rafique, et al.
Materials (Basel, Switzerland)
|
November 11, 2022
Prediction of Autogenous Shrinkage of Concrete Incorporating Super Absorbent Polymer and Waste Materials through Individual and Ensemble Machine Learning Approaches
Hisham Jahangir Qureshi, Muhammad Umair Saleem, Muhammad Faisal Javed, et al.
Transplantation and Cellular Therapy
|
January 4, 2025
Outcomes of Allogeneic Hematopoietic Stem Cell Transplantation in Patients Aged 70 Years and Older: A Systematic Review and Meta-Analysis
Moazzam Shahzad, Qamar Iqbal, Muhammad Kashif Amin, et al.
Academic Radiology
|
February 1, 2025
Cardiac Amyloidosis: A Comprehensive Review of Imaging Findings
Alireza Mohseni, Ghazal Zandieh, Kristin Porter, et al.
BMC Plant Biology
|
July 26, 2024
Multiple cropping effectively increases soil bacterial diversity, community abundance and soil fertility of paddy fields
Haiying Tang, Ying Liu, Xiaoqi Yang, et al.
Ticks and Tick-Borne Diseases
|
April 30, 2023
First molecular confirmation of multiple zoonotic vector-borne diseases in pet dogs and cats of Hong Kong SAR
Sabir Hussain, Abrar Hussain, Muhammad Umair Aziz, et al.
Sensors (Basel, Switzerland)
|
April 12, 2022
Modeling of Efficient Control Strategies for LCC-HVDC Systems: A Case Study of Matiari-Lahore HVDC Power Transmission Line
Adeel Ahmed, Danish Khan, Ahmed Muddassir Khan, et al.
Frontiers in Pediatrics
|
September 27, 2019
Biallelic Missense Mutation in the <i>ECEL1</i> Underlies Distal Arthrogryposis Type 5 (DA5D)
Muhammad Umair, Amjad Khan, Amir Hayat, et al.
Molecular Syndromology
|
April 3, 2025
A Novel Loss of Function Variant in <i>HCN1</i> Gene Underlies Early Infantile Epileptic Encephalopathy 24 [EIEE24]
Mujahid, Ahmed Waqas, Ibrahim A Almazni, et al.
Page
of 117