Genetic Risk Score Constructed from Polymorphisms in the VEGFA, TBX5, and SMAD7 Genes Provides Novel Insights into the Molecular Mechanisms of the Tetralogy of Fallot and Ventricul... von Ashiq, Sana, Sabar, Muhammad Farooq, Hyder, Syed Najam

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Familial DNA analysis and criminal investigation: Usage, downsides and privacy concerns von Mateen, Rana Muhammad, Sabar, Muhammad Farooq, Hussain, Safdar, Parveen, Rukhsana, Hussain, Manzoor

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Dilemmas in the Diagnosis and Management of CML in Pakistan von Khan, Sahrish, Sabar, Muhammad Farooq, Akbar, Mariyam, Waris, Abdul

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Role of Vascular Endothelial Growth Factor as a Potential Biomarker in Congenital Heart Defects: A Systematic Review von Ashiq, Sana, Hyder, Syed Najam, Ashiq, Kanwal, Sabar, Muhammad Farooq

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Prevention programmes and prenatal diagnosis for beta thalassemia in Pakistan: A narrative review von Ghafoor, Mahmood, Sabar, Muhammad Farooq, Sabir, Furqan

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The role of NKX2-5 gene polymorphisms in congenital heart disease (CHD): a systematic review and meta-analysis von Ashiq, Sana, Ashiq, Kanwal, Sabar, Muhammad Farooq

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The impact of COVID-19 on asthma patients: current knowledge and future perspective von Sabar, Muhammad Farooq, Ashiq, Sana, Shahid, Mariam

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Identification of Prognostic Genes Associated with Asthma in Pakistan von Naeem, Faiza, Sabar, Muhammad Farooq, Ghani, Muhammad Usman, Ain, Qurat Ul, Zafar, Qurat-ul-Ain

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Forensic and Genetic Characterization of mtDNA Lineages of Shin, a Unique Ethnic Group in Pakistan von Khan, Muhammad Umer, Sabar, Muhammad Farooq, Baig, Atif Amin, Naqvi, Arif-un-Nisa, Ghani, Muhammad Usman

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Major histocompatibility complex class II polymorphic variants are associated with asthma predisposition in the Punjabi population of Lahore, Pakistan von Aslam, Raheela, Shahid, Mariam, Bano, Iqbal, Ayoub, Muhammad, Sabar, Muhammad Farooq, Altaf, Saba, Kousar, Samra, Ghani, Muhammad Usman, Husnain, Tayyab, Shahid, Ahmad Ali

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P258: Diversity of CFTR mutations in a Pakistani population: Implications for comprehensive genetic testing and genetic counseling in cystic fibrosis von Safdar, Anum, Ghani, Muhammad Usman, Bano, Iqbal, Mehmood, Tahir, Akbar, Ali, Awan, Farheena Iqbal, Rafique, Hassan, Sabar, Muhammad Farooq, Tajamal, Muhammad, Shaikh, Rehan Sadiq

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Integrated Genomic Analysis Identifies ANKRD36 Gene as a Novel and Common Biomarker of Disease Progression in Chronic Myeloid Leukemia von Iqbal, Zafar, Absar, Muhammad, Akhtar, Tanveer, Aleem, Aamer, Jameel, Abid, Basit, Sulman, Ullah, Anhar, Afzal, Sibtain, Ramzan, Khushnooda, Rasool, Mahmood, Karim, Sajjad, Mirza, Zeenat, Iqbal, Mudassar, AlMajed, Maryam, AlShehab, Buthinah, AlMukhaylid, Sarah, AlMutairi, Nouf, Al-anazi, Nawaf, Sabar, Muhammad Farooq, Arshad, Muhammad, Asif, Muhammad, Shammas, Masood, Mahmood, Amer

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Awareness of Asthma Genetics in Pakistan: A Review with Some Recommendations von Muhammad Farooq Sabar, Muhammad Akram, Farheena Iqbal Awan, Muhammad Usman Ghani, Mariam Shahid, Zafar Iqbal, Samra Kousar, Muhammad Idrees

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Association of maternal hypertension and diabetes with variants of the NKX2-5, LEFTY1 and LEFTY2 genes in children with congenital heart defects: a case-control study from Pakistan... von Ashiq, Sana, Sabar, Muhammad Farooq

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Role of Molecular Biology in Cancer Treatment: A Review Article von Imran, Aman, Qamar, Hafiza Yasara, Ali, Qurban, Naeem, Hafsa, Riaz, Mariam, Amin, Saima, Kanwal, Naila, Ali, Fawad, Sabar, Muhammad Farooq, Nasir, Idrees Ahmad

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A report on asthma genetics studies in Pakistani population von Muhammad Usman Ghani, Muhammad Farooq Sabar, Mariam Shahid, Farheena Iqbal Awan, Muhammad Akram

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ROLE OF SINGLE-NUCLEOTIDE VARIATIONS OF TSLP IN ASTHMA DISEASE von ULLAH, RAHMAT, MEHDI, ZOHAIR, GHANI, MUHAMMAD USMAN, FAROOQ SABAR, MUHAMMAD, UMER KHAN, MUHAMMAD

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SNP VARIANTS OF IL-27 GENE AS GENOMIC PREDICTORS AGAINST EFFECTIVENESS OF VITAMIN-D THERAPY IN COPD PATIENTS von USMAN GHANI, MUHAMMAD, FAROOQ SABAR, MUHAMMAD, SHAHID, MARIAM, AKRAM, MUHAMMAD, ANWAR, BILAL, ANWAR, MUHAMMAD BURHAN

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Dilemma in Diagnosis and Management of CML in Pakistan von Khan, Sahrish, Sabar, Muhammad Farooq, Akbar, Mariyam, Waris, Abdul

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A New Locus for Autosomal Recessive Nuclear Cataract Mapped to Chromosome 19q13 in a Pakistani Family von Riazuddin, S. Amer, Yasmeen, Afshan, Zhang, Qingjiong, Yao, Wenliang, Sabar, Muhammad Farooq, Ahmed, Zahoor, Riazuddin, Sheikh, Hejtmancik, J. Fielding

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