Search Results - Naveed Wasif
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1
A Novel Homozygous Frameshift Mutation in CCN6 Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family by Nagwa E. A. Gaboon, Asia Parveen, Asia Parveen, Ahmed El Beheiry, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Mosab S. Alsaedi, Naveed Wasif, Naveed Wasif, Naveed Wasif
Published 2019Call Number: Loading…Connect to this object online.
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2
A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients by Nagwa E. A. Gaboon, Asia Parveen, Asia Parveen, Khaled A. Ahmad, Taghreed Shuaib, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Lereen Abdelwehab, Amina Arif, Naveed Wasif, Naveed Wasif, Naveed Wasif
Published 2020Call Number: Loading…Connect to this object online.
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3
Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa by Fozia Fozia, Fozia Fozia, Rubina Nazli, Nousheen Bibi, Sher Alam Khan, Noor Muhammad, Nafila Shakeeb, Saadullah Khan, Musharraf Jelani, Naveed Wasif, Naveed Wasif
Published 2021Call Number: Loading…Connect to this object online.
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4
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family by Sher Alam Khan, Muhammad Adnan Khan, Nazif Muhammad, Hina Bashir, Niamat Khan, Noor Muhammad, Rüstem Yilmaz, Saadullah Khan, Naveed Wasif
Published 2020Call Number: Loading…Connect to this object online.
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5
Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families by Syeda Iqra Hussain, Nazif Muhammad, Shahbaz Ali Shah, Adil u Rehman, Sher Alam Khan, Shamim Saleha, Yar Muhammad Khan, Noor Muhammad, Saadullah Khan, Naveed Wasif
Published 2024Call Number: Loading…Connect to this object online.
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