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Publications by J. W. Lin
DNA Sequence Analysis and Genotype-Phenotype Assessment in 71 Patients With Syndromic Hearing Loss or Auditory Neuropathy
BMJ Open
Medicine
Local Bonds Anomalies and Dynamics in Bismuth Ferrite
AIP Advances
Nanotechnology
Astronomy
Physics
Nanoscience
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Genotype-Phenotype Correlation Analysis of MYO15A Variants in Autosomal Recessive Non-Syndromic Hearing Loss
BMC Medical Genetics
Genetics
Genotype-Phenotype Correlation in Hereditary Hearing Loss
Comprehensive Analysis of Syndromic Hearing Loss Patients in Japan
Scientific Reports
Multidisciplinary
Amelogenesis Imperfecta: Genotype-Phenotype Studies in 71 Families
Cells Tissues Organs
Anatomy
Histology
Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss
Revista Romana de Medicina de Laborator
Electrophysiological Assessment of Auditory Processing Disorder in Children With Non-Syndromic Cleft Lip and/or Palate
PeerJ
Genetics
Molecular Biology
Biochemistry
Biological Sciences
Medicine
Agricultural
Neuroscience
Which Patients With a Unilateral Hearing Aid for Symmetric Sensorineural Hearing Loss Have Auditory Deprivation?
Clinical and Experimental Otorhinolaryngology
Otorhinolaryngology
Surgery