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Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.

Brittany T TruongTalitha K L YarzaTori Bootpetch RobertsSusannah RobertsJonathan XuMatthew J SteritzCelina A M Tobias-GrassoMahshid AzamianSeema R LalaniKaren L MohlkeNanette R LeeEva Maria Cutiongco-de la PazMaria Rina T Reyes-QuintosRegie Lyn P Santos-CortezCharlotte M Chiong
Published in: Clinical genetics (2019)
Keyphrases
  • hearing loss
  • copy number
  • single cell
  • genome wide
  • dna methylation