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Simeen-ber-Rahman

Showing results (21-30 of 26) with videos related to

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Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|September 19, 2008
Familial dysbetalipoproteinemia: a potentially fatal disorderArfan Ul Bari, Rizwan Hashim, Simeen Ber Rahman, et al.
International Archives of Allergy and Immunology|November 16, 2022
The Association of HLA Alleles and Haplotypes with Age of Disease Onset in Pakistani Psoriatic PatientsSaeeda Munir, Simeen Ber Rahman, Sadia Rehman, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|July 2, 2004
Neurofibromatosis and Caroli's disease: an extremely rare associationArfan ul Bari, Tariq Mehmood, Shahid H Hussain, et al.
Congenital Anomalies|June 24, 2018
Identification and association of recurrent ALOXE3 mutation with non-bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani familiesSimeen Ber Rahman, Asif Mir, Nafees Ahmad, et al.
Molecular Immunology|December 8, 2014
Association analysis of GWAS and candidate gene loci in a Pakistani population with psoriasisSaeeda Munir, Simeen ber Rahman, Sadia Rehman, et al.
Molecular Biology Reports|January 14, 2014
Identification of recurrent c.742G>T nonsense mutation in ECM1 in Pakistani families suffering from lipoid proteinosisMuhammad Nasir, Simeen Ber Rahman, Christian M K Sieber, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|September 19, 2008
Familial dysbetalipoproteinemia: a potentially fatal disorderArfan Ul Bari, Rizwan Hashim, Simeen Ber Rahman, et al.
International Archives of Allergy and Immunology|November 16, 2022
The Association of HLA Alleles and Haplotypes with Age of Disease Onset in Pakistani Psoriatic PatientsSaeeda Munir, Simeen Ber Rahman, Sadia Rehman, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|July 2, 2004
Neurofibromatosis and Caroli's disease: an extremely rare associationArfan ul Bari, Tariq Mehmood, Shahid H Hussain, et al.
Congenital Anomalies|June 24, 2018
Identification and association of recurrent ALOXE3 mutation with non-bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani familiesSimeen Ber Rahman, Asif Mir, Nafees Ahmad, et al.
Molecular Immunology|December 8, 2014
Association analysis of GWAS and candidate gene loci in a Pakistani population with psoriasisSaeeda Munir, Simeen ber Rahman, Sadia Rehman, et al.
Molecular Biology Reports|January 14, 2014
Identification of recurrent c.742G>T nonsense mutation in ECM1 in Pakistani families suffering from lipoid proteinosisMuhammad Nasir, Simeen Ber Rahman, Christian M K Sieber, et al.
Pageof 3