Analysis of FANCC gene mutations (IVS4+4A>T, del322G ...
journals.tubitak.gov.tr
by I AFTAB · · Cited by 11 — SHAGUFTA KHALIQ · SHAHIDA MOHSIN. DOI sag Abstract. Background/aim: Fanconi anemia (FA) is an autosomal recessive disease determined by ... › medical › vol47 › iss2
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KHALIQ, Shagufta: مفت ڈاؤنلوڈ. ای بک لائبریری۔ Z-Library پر آن لائن ...
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Qasim Ayub, Atika Mansoor, Muhammad Ismail, Shagufta Khaliq, Aisha Mohyuddin, Abdul Hameed, Kehkashan Mazhar, Sadia Rehman, Saima Siddiqi, Myrto Papaioannou ... › author
Syed Qasim Mehdi: مفت ڈاؤنلوڈ. ای بک لائبریری۔ Z-Library پر آن ...
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Sadaf Firasat, Ali Raza, Aiysha Abid, Tahir Aziz, Mohammad Mubarak, Syed Ali Anwar Naqvi, Syed Adeebul Hasan Rizvi, Syed Qasim Mehdi, Shagufta Khaliq. › author
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PakMediNet - Authors Index
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Pakistans First Largest Medical Database containing Research Articles Published in Pakistani Medical Journals, Database of Medical Journals and Pakistani...
ATOH7 mutations cause autosomal recessive persistent ...
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by L Prasov · · Cited by 68 — Shagufta Khaliq,. Shagufta Khaliq. 3. Department of Human Genetics and Molecular Biology. ,. University of Health Sciences. › hmg › article-abstract
linkage to 9q and germline HSF4 mutations - ProQuest
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by T Forshew · · Cited by 81 — Tim Forshew Ж Colin A. Johnson Ж Shagufta Khaliq. Shanaz Pasha Ж Catherine Willis Ж Rashida Abbasi. Louise Tee Ж Ursula Smith Ж Richard C. Trembath. › openview › 1.pdf
Refinement of the locus for autosomal recessive cone-rod ...
pubmed.ncbi.nlm.nih.gov
by M Ismail · · Cited by 15 — Authors. Muhammad Ismail , Aiysha Abid , Khalid Anwar , S Qasim Mehdi , Shagufta Khaliq. Affiliations. 1 Biomedical and Genetic Engineering Division, ... by A Abid — Authors. Aiysha Abid , Ali Raza , Tahir Aziz , Shagufta Khaliq. Affiliations. 1 Centre for Human Genetics and Molecular Medicine, ... › ...
Osteopontin promoter polymorphisms and risk of urolithiasis
bmcmedgenet.biomedcentral.com
by A Amar · · Cited by 3 — Ali Amar, Ayesha Afzal, Humaira Najma & Shagufta Khaliq. Department of Urology, Fatima Jinnah Medical University, Lahore, Punjab, Pakistan. › articles
Y-chromosomal evidence for a limited Greek contribution to ...
www.nature.com
by S Firasat · · Cited by 90 — Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan. Sadaf Firasat,; Shagufta Khaliq, ... › ... › articles
All web results to the name "Shagufta Khaliq"
A spectrum of novel NPHS1 and NPHS2 gene mutations in ...
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by A Abid · · Cited by 57 — Shagufta Khaliq. Centre for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation, Karachi, Pakistan ... › resource
Association of a Single-Nucleotide Polymorphism in the ...
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by S Ajaz · · Cited by 38 — Sadia Ajaz · Shagufta Khaliq · Aiysha Abid · Asad Shehzad Hassan · Altaf Hashmi · Gauhar Sultan · Rehan Mohsin · Mohammad Mubarrak ... › doi › abs › gtmb
Relationship between IQ and academic performance of ...
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by K Iqbal · · Cited by 2 — Shagufta Khaliq Lahore Medical & Dental College, Lahore. Muneeza Taseer Ameer ud Din Medical College, PGMI, Lahore. › tpmj › article › view
The Kalash genetic isolate: ancient divergence, drift, and ...
europepmc.org
by Q Ayub · · Cited by 54 — Massimo Mezzavilla,1,2,7 Luca Pagani,1,3 Marc Haber,1 Aisha Mohyuddin,4Shagufta Khaliq,5 Syed Qasim Mehdi,6 and Chris Tyler-Smith › article › pmc
Shagufta Khaliq - Google Scholar Citationsscholar.google.com/citations?user=mMWJ00sAAAAJ&hl=en
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View all. Follow. Shagufta Khaliq. UHS, Lahore. Verified email at uhs.edu.pk. Human Disease Genetics & Population Genetics. ArticlesCited byCo-authors ...
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