Jabbar Khan
Dera Ismail Khan, KP 29050, Pakistan
Last Updated: 09/26/2026
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Found 11 publications
Protein truncating splice site variant in ALDH1A3 associated with bilateral anophthalmia identified in a multiplex consanguineous Pakistani family.
Journal: International journal of ophthalmology
Published: March 11, 2025
A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.
Journal: Genetics and molecular biology
Published: February 13, 2025
Current updates on genetic spectrum of usher syndrome.
Journal: Nucleosides, nucleotides & nucleic acids
Published: May 08, 2024
A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome.
Journal: Bone reports
Published: May 03, 2024
Wild Edible Fruits as a Source of Food and Medicine: A Study among Tribal Communities of Southern Khyber Pakhtunkhwa.
Journal: Plants (Basel, Switzerland)
Published: November 02, 2023
Genetic basis of ß-thalassemia in families of pashtun ethnicity in Dera Ismail Khan district of Khyber Pakhtun-Khwa province, Pakistan.
Journal: Expert review of hematology
Published: July 26, 2023
Epstein - Barr virus epidemiology in HIV infected transsexuals.
Journal: JPMA. The Journal of the Pakistan Medical Association
Published: August 21, 2021
Consanguinity, the driving force behind inheritance of HbS-β thalassemia in Southern Districts of KP.
Journal: JPMA. The Journal of the Pakistan Medical Association
Published: August 19, 2020
Genetic determinants of β-thalassemia intermedia in Pakistan.
Journal: Hemoglobin
Published: February 25, 2015
Showing 1-11 of 11
Last Updated: 09/26/2026