Search

Search Constraints

You searched for: Author/Creator Riazuddin, Sheikh

Search Results

1. A mutation in IFT43 causes non-syndromic recessive retinal degeneration. (18th September 2017)

3. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes. Issue 11 (22nd September 2011)

9. Genetic Analysis through OtoSeq of Pakistani Families Segregating Prelingual Hearing Loss. Issue 3 (14th June 2013)

10. Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss. Issue 1 (18th November 2018)