Zobrazeno 1 - 10
of 214
pro vyhledávání: '"Sher, Alam"'
Autor:
Syeda Iqra Hussain, Nazif Muhammad, Shahbaz Ali Shah, Adil u Rehman, Sher Alam Khan, Shamim Saleha, Yar Muhammad Khan, Noor Muhammad, Saadullah Khan, Naveed Wasif
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background Intellectual disability (ID) is a neurodevelopmental condition affecting around 2% of children and young adults worldwide, characterized by deficits in intellectual functioning and adaptive behavior. Genetic factors contribute to
Externí odkaz:
https://doaj.org/article/0bf506cd157941d9a08ba30ae9d314c0
Autor:
Sher, Alam, Noor, Mehmood Ali, Li, Hong Xing, Nasir, Bukhtawer, Manzoor, Muhammad Aamir, Hussain, Saddam, Zhang, Jiwang, Riaz, Muhammad Waheed, Hussain, Shabbir
Publikováno v:
In Plant Stress September 2024 13
Autor:
Syeda Iqra Hussain, Nazif Muhammad, Salah Ud Din Shah, Fardous Fardous, Sher Alam Khan, Niamatullah Khan, Adil U Rehman, Mehwish Siddique, Shoukat Ali Wasan, Rooh Niaz, Hafiz Ullah, Niamat Khan, Noor Muhammad, Muhammad Usman Mirza, Naveed Wasif, Saadullah Khan
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Intellectual disability (ID) is a condition that varies widely in both its clinical presentation and its genetic underpinnings. It significantly impacts patients’ learning capacities and lowers their IQ below 70. The solute carr
Externí odkaz:
https://doaj.org/article/182d292c0a164356a02dec76b2700079
Autor:
Nawaz, Hamed, Parveen, Asia, Khan, Sher Alam, Zalan, Abul Khair, Khan, Muhammad Adnan, Muhammad, Noor, Hassib, Nehal F., Mostafa, Mostafa I., Elhossini, Rasha M., Roshdy, Nehal Nabil, Ullah, Asmat, Arif, Amina, Khan, Saadullah, Ammerpohl, Ole, Wasif, Naveed
Publikováno v:
In Heliyon 15 January 2024 10(1)
Autor:
Hamed Nawaz, Asia Parveen, Sher Alam Khan, Abul Khair Zalan, Muhammad Adnan Khan, Noor Muhammad, Nehal F. Hassib, Mostafa I. Mostafa, Rasha M. Elhossini, Nehal Nabil Roshdy, Asmat Ullah, Amina Arif, Saadullah Khan, Ole Ammerpohl, Naveed Wasif
Publikováno v:
Heliyon, Vol 10, Iss 1, Pp e23688- (2024)
Brachyolmia is a heterogeneous group of developmental disorders characterized by a short trunk, short stature, scoliosis, and generalized platyspondyly without significant deformities in the long bones. DASS (Dental Abnormalities and Short Stature),
Externí odkaz:
https://doaj.org/article/0f91f966fd7d4676bcf74cad84128e34
Publikováno v:
Human Genome Variation, Vol 10, Iss 1, Pp 1-3 (2023)
Abstract Split-hand/foot malformation (SHFM) shows diverse heterogeneity and manifests with reduced penetrance and variable expressivity. This study investigated the underlying genetic cause of a family segregating SHFM. Exome sequencing followed by
Externí odkaz:
https://doaj.org/article/334e8e58bdef4ab3be75b7c0dc035b67
Akademický článek
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Autor:
Nazif Muhammad, Syeda Iqra Hussain, Zia Ur Rehman, Sher Alam Khan, Samin Jan, Niamatullah Khan, Muhammad Muzammal, Sumra Wajid Abbasi, Naseebullah Kakar, Muzammil Ahmad Khan, Muhammad Usman Mirza, Noor Muhammad, Saadullah Khan, Naveed Wasif
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionIntellectual disability (ID) is a clinically and genetically heterogeneous disorder. It drastically affects the learning capabilities of patients and eventually reduces their IQ level below 70.MethodsThe current genetic study ascertained
Externí odkaz:
https://doaj.org/article/6f43da395223452583503bcd265ce47a
Publikováno v:
Discover Sustainability; 12/4/2024, Vol. 5 Issue 1, p1-23, 23p
Autor:
Sher, Alam, Mudassir Maqbool, Muhammad, Iqbal, Javed, Nadeem, Muhammad, Faiz, Sajid, Noor, Hafeez, Hamid, Yasir, Yuan, Xiangyang, pingyi, Guo
Publikováno v:
In Saudi Journal of Biological Sciences November 2021 28(11):6471-6479