Publication | Open Access
Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss
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Citations
24
References
2015
Year
Dfnb49 Hearing LossMendelian DisorderGenetic DisorderGeneticsAudiologySlovak FamiliesClinical PhenotypeAuditory ScienceHuman HearingArtsMedicineClinical GeneticsHearing Loss
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