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Saima Riazuddin

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Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population

2012 Orphanet Journal of Rare Diseases
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USH1K , a novel locus for type I Usher syndrome, maps to chromosome 10p11.21–q21.1

2012 Journal of Human Genetics
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Genetic and Molecular Basis of Nonsyndromic Deafness.

2001
- Saima Riazuddin
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