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Publications by M. KHALIL
Screening of the Connexin 26 (35delg) Mutation in Egyptian Patients With Autosomal Recessive Nonsyndromic Deafness and Its Relation to the Patients' Iq
Egyptian Journal of Genetics and Cytology
Related publications
Frequency of C.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients With Nonsyndromic Hearing Impairment
Genetics Research International
Genetics
Molecular Biology
Screening of Connexin 26 in Nonsyndromic Hearing Loss
International Archives of Otorhinolaryngology
Otorhinolaryngology
Comprehensive Analysis of Deafness Genes in Families With Autosomal Recessive Nonsyndromic Hearing Loss
PLoS ONE
Multidisciplinary
Mapping of a Novel Autosomal Recessive Nonsyndromic Deafness Locus (DFNB46) to Chromosome 18p11.32-P11.31
American Journal of Medical Genetics, Part A
Genetics
Mutation Screening of Multiple Genes in Spanish Patients With Autosomal Recessive Retinitis Pigmentosa by Targeted Resequencing
PLoS ONE
Multidisciplinary
A Common Founder for the 35delG GJB2 Gene Mutation in Connexin 26 Hearing Impairment
Journal of Medical Genetics
Genetics
Unauffälliges UNHS-Screening Bei Einem Homozygoten Träger Der 35delG-Mutation Im Connexin 26 Kodierenden Gjb2-Gen
Monatsschrift fur Kinderheilkunde
Child Health
Surgery
Pediatrics
Perinatology
Birth Prevalence and Mutation Spectrum in Danish Patients With Autosomal Recessive Albinism
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Substitutions in the Conserved C2C Domain of Otoferlin Cause DFNB9, a Form of Nonsyndromic Autosomal Recessive Deafness
Neurobiology of Disease
Neurology
