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Browsing by Author Qasim, M.
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| Full Text | Issue Date | Title | Author(s) | | 2008 | Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome. | Ahmed, Z.M.; Riazuddin, Saima; Aye, S.; Ali, R.A.; Venselaar, H., et al |
| 2012 | Targeted next generation sequencing reveals a novel intragenic deletion of the TPO gene in a family with intellectual disability | Iqbal, Z.; Neveling, K.; Razzaq, A.; Shahzad, M.; Zahoor, M.Y., et al |
Showing results 1 to 2 of 2
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