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Publications by Michael Kovasala
Analyses of Del(GJB6‐D13S1830) and Del(GJB6‐D13S1834) Deletions in a Large Cohort With Hearing Loss: Caveats to Interpretation of Molecular Test Results in Multiplex Families
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Related publications
Absence of GJB2 Gene Mutations, the GJB6 Deletion (GJB6-D13S1830) and Four Common Mitochondrial Mutations in Nonsyndromic Genetic Hearing Loss in a South African Population
International Journal of Pediatric Otorhinolaryngology
Medicine
Otorhinolaryngology
Pediatrics
Perinatology
Child Health
GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss
Revista Romana de Medicina de Laborator
GJB3 /GJB6 Screening in GJB2 Carriers With Idiopathic Hearing Loss: Is It Necessary?
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
Screening of GJB6 Gene for the 342-Kb Deletion in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
SCA15 Due to Large ITPR1 Deletions in a Cohort of 333 White Families With Dominant Ataxia
Archives of Neurology
Contribution of SLC26A4 to the Molecular Diagnosis of Nonsyndromic Prelingual Sensorineural Hearing Loss in a Brazilian Cohort
BMC Research Notes
Biochemistry
Medicine
Genetics
Molecular Biology
Frequency of GJB 2 Mutations, GJB 6‐D13S1830 and GJB 6‐D13S1854 Deletions Among Patients With Non‐syndromic Hearing Loss From the Central Region of Iran
Molecular genetics & genomic medicine
Genetics
Molecular Biology
A Recurrent Missense Variant in HARS2 Results in Variable Sensorineural Hearing Loss in Three Unrelated Families
Journal of Human Genetics
Genetics
Families of Children With Hearing Loss and Parental Educational Practices
