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Publications by Guney Bademci
De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
American Journal of Human Genetics
Genetics
Dysfunction of GRAP, Encoding the GRB2-related Adaptor Protein, Is Linked to Sensorineural Hearing Loss
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Identification of Candidate Gene FAM183A and Novel Pathogenic Variants in Known Genes: High Genetic Heterogeneity for Autosomal Recessive Intellectual Disability
PLoS ONE
Multidisciplinary
Comprehensive Analysis of Deafness Genes in Families With Autosomal Recessive Nonsyndromic Hearing Loss
PLoS ONE
Multidisciplinary
Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53
Molecular Genetics and Genomics
Medicine
Genetics
Molecular Biology
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
Common Genes for Non-Syndromic Deafness Are Uncommon in Sub-Saharan Africa: A Report From Nigeria
International Journal of Pediatric Otorhinolaryngology
Medicine
Otorhinolaryngology
Pediatrics
Perinatology
Child Health
Evaluation of the Results of Cordocentesis; 9 Years Experience
Turk Jinekoloji ve Obstetrik Dernegi Dergisi
Gynecology
Obstetrics
