Fingerprint
Dive into the research topics of 'Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss
Gowri Nayak, Lukas Varga, Claire Trincot, Mohsin Shahzad, Penelope L. Friedman, Iwar Klimes, John H. Greinwald, S. Amer Riazuddin, Ivica Masindova, Milan Profant, Shaheen N. Khan, Thomas B. Friedman, Zubair M. Ahmed, Daniela Gasperikova, Sheikh Riazuddin, Saima Riazuddin
Research output: Contribution to journal › Article › peer-review
11
Scopus
citations