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Shehla Anjum Baig
Shehla Anjum Baig
Pakistan Institute of Medical Sciences
Missense mutation
Genetics
Biology
Gene
Dominance (genetics)
4
Papers
44
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Whole exome sequencing identifies LRP1 as a pathogenic gene in autosomal recessive keratosis pilaris atrophicans
2015
Journal of Medical Genetics
Joakim Klar
Jens Schuster
Tahir Naeem Khan
Muhammad Jameel
Katrin Mäbert
Lars Forsberg
Shehla Anjum Baig
Shahid Mahmood Baig
Niklas Dahl
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Citations (8)
Evidence for autosomal recessive inheritance in SPG3A caused by homozygosity for a novel ATL1 missense mutation
2014
European Journal of Human Genetics
Tahir Naeem Khan
Joakim Klar
Muhammad Tariq
Shehla Anjum Baig
Naveed Altaf Malik
Raja Yousaf
Shahid Mahmood Baig
Niklas Dahl
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Citations (28)
β-Thalassemia in Pakistan: a pilot program on prenatal diagnosis in Multan.
2012
Journal of Pediatric Hematology Oncology
Mahmood Baig S
Sabih D
Rahim Mk
Aysha Azhar
Muhammad Tariq
Sajid Hussain M
Saqlan Naqvi Sm
Ghazala Kaukab Raja
Tahir Naeem Khan
Muhammad Jameel
Iram Z
Noor S
Baig Ur
Javed Anver Qureshi
Shehla Anjum Baig
Syeda Marriam Bakhtiar
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Citations (7)
Report of a recurrent mutation in ARS (component B) gene with severe Mal de Meleda in a large consanguineous Pakistani family
2011
Journal of the Medical Sciences
Sadia Nawaz
Muhammad Tariq
Aysha Azhar
Mahmood Rasool
Syeda Marriam Bakhtiar
Ilyas Ahmad
Shoaib ur Rehman
Muhammad Jameel
Tahir Naeem Khan
Shehla Anjum Baig
Joakim Klar
Niklas Dahl
Shahid Mahmood Baig
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