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Publications by V Migliosi
Q829X, a Novel Mutation in the Gene Encoding Otoferlin (OTOF), Is Frequently Found in Spanish Patients With Prelingual Non-Syndromic Hearing Loss
Journal of Medical Genetics
Genetics
Related publications
Non-Syndromic Recessive Auditory Neuropathy Is the Result of Mutations in the Otoferlin (OTOF) Gene
Journal of Medical Genetics
Genetics
Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Application of Allele-Specific Primer Extension-Based Microarray for Simultaneous Multi-Gene Mutation Screening in Patients With Non-Syndromic Hearing Loss
International Journal of Molecular Medicine
Medicine
Genetics
Identification of a Novel Homozygous Mutation, TMPRSS3: C.535G>A, in a Tibetan Family With Autosomal Recessive Non-Syndromic Hearing Loss
PLoS ONE
Multidisciplinary
TBL1Y: A New Gene Involved in Syndromic Hearing Loss
European Journal of Human Genetics
Genetics
Novel Recessive PDZD7 Biallelic Mutations in Two Chinese Families With Non-Syndromic Hearing Loss
American Journal of Medical Genetics, Part A
Genetics
Screening of GJB6 Gene for the 342-Kb Deletion in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss
Zahedan Journal of Research in Medical Sciences
Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
