Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Zamrud Zehri"'
Autor:
Tayyaba Afsar, Hongxia Fu, Hammal Khan, Zain Ali, Zamrud Zehri, Gohar Zaman, Safdar Abbas, Arif Mahmood, Qamre Alam, Junjian Hu, Suhail Razak, Muhammad Umair
Publikováno v:
Frontiers in Genetics, Vol 14 (2024)
Background: Neurodevelopmental disorders are characterized by different combinations of intellectual disability (ID), communication and social skills deficits, and delays in achieving motor or language milestones. SLITRK2 is a postsynaptic cell-adhes
Externí odkaz:
https://doaj.org/article/2824b0791d5a4f9aa0d463705e6ae6d2
Autor:
Anam Nayab, Shagufta Andleeb, Shah Zeb, Hafiza Yasmin Manzoor, Zamrud Zehri, Arif Mahmood, Hammal Khan, Muhammad Umair, Ahmed Waqas
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 6, Iss 1, Pp 22-28 (2023)
Background: Glycosylphosphatidylinositol (GPI) is a glycolipid containing phosphatidylinositol related to the protein surfaces by covalent attachment. Inherited GPI deficiencies have various phenotypic chrematistics, which range from intellectual dis
Externí odkaz:
https://doaj.org/article/b7f46a48c0524dd1b05fa88a0a857f32
Autor:
Muhammad Bilal, Muhammad Raheel, Gul Hassan, Shah Zeb, Arif Mahmood, Zamrud Zehri, Hafiza Yasmin Manzoor, Muhammad Umair
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 6, Iss 1, Pp 29-35 (2023)
Background: Polydactyly or hexadactyly is a familiar limb defect that either occurs as an isolated entity (non-syndromic) or is associated with severe (syndromic) morphological phenotypes. Generally, it appears due to a defect in the anteroposterior
Externí odkaz:
https://doaj.org/article/da295602d659419b8349b36ffd752bf8
Autor:
Ahmed Waqas, Romana Liaqat, Sidrah Shaheen, Ali Zaman Khan, null Mujahid, Alaa Hamed Habib, Najat Binothman, Majidah Aljadani, Zamrud Zehri, Shabnam Shaheen, Afnan Alkathiri, Rubina Naz, Muhammad Umair, Safdar Abbas
Publikováno v:
International Journal of Developmental Neuroscience. 83:191-200
Neurodevelopmental disorders (NDDs) are classified as a group of disorders affecting function and development of the brain and having wide clinical variability. Herein, we describe two affected individuals segregating a recessive NDD. The affected in