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The Research Papers for the Researcher
Dr. Sadia Nawaz


2012
Nawaz, S., Tariq, M., Ahmad, I., Malik NA, Baig, SM, Klar J. and Dahl, N. . Non-bullous congentital ichthyosiform erythroderma associated with homozygosity for a novel missense mutation in an ATP binding domain of ABCA12. European journal of dermatology: EJD ;22((2)):178-181.
Khan TN, Nawaz S, Klar J, Jameel M, Tariq M, Malik NA, Baig SM, Dahl N.. Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I). . BMC Med Genet. ;13((1):):
2011
Fro¨jmark AS, Schuster J, Sobol M, Entesarian M, Kilander MBC, Gabrikova D, Nawaz S, Baig SM, Schulte G, Klar J, and Dahl N.. Mutations in Frizzled 6 Cause Isolated Autosomal-Recessive Nail Dysplasia. . The American Journal of Human Genetics. ;88():852-60
Nawaz S, Tariq M, Azhar A, Rasool M, Bakhtiar SM, Ahmad I, ur Rehman S, Jameel M, Khan TN, Baig SA, Klar J, Dahl N, Baig SM. . Report of a recurrent mutation in ARS (component B) gene with severe Mal de Meleda in a large consanguineous Pakistani family.. Pak J Med Sci (Part-II);27(3):686-689
2010
Rasool M, Nawaz S, Azhar A, Wajid M, Westermark P, Baig SM, Klar J, Dahl N. . Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation. . Eur J Dermatol ;20(4):443-6
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