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Publications by Jonathan C. Stephens
A Gain-Of-Function Variant in DIAPH1 Causes Dominant Macrothrombocytopenia and Hearing Loss
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Construction and Phase I Clinical Evaluation of the Safety and Immunogenicity of a Candidate Enterotoxigenic Escherichia Coli Vaccine Strain Expressing Colonization Factor Antigen CFA/I
Infection and Immunity
Parasitology
Infectious Diseases
Immunology
Microbiology
Related publications
Treatment of Hearing Gain in Failed Idiopathic Sudden Sensorineural Hearing Loss
Otolaryngology - Head and Neck Surgery
Otorhinolaryngology
Surgery
A Gain-Of-Function Mutation in theGRIK2gene Causes Neurodevelopmental Deficits
Neurology: Genetics
Neurology
Genetics
Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss
Otology and Neurotology
Medicine
Otorhinolaryngology
Sensory Systems
Neurology
Gain-Of-Function Mutation in Gli3 Causes Ventricular Septal Defects
A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
Loss of OATP1B3 Function Causes Rotor Syndrome
Cancer Biology and Therapy
Cancer Research
Oncology
Molecular Medicine
Pharmacology
A Novel Mutation in FGFR3 Causes Camptodactyly, Tall Stature, and Hearing Loss (CATSHL) Syndrome
American Journal of Human Genetics
Genetics
A C-Terminal Nonsense Mutation Links PTPRQ With Autosomal-Dominant Hearing Loss, DFNA73
Genetics in Medicine
Medicine
Genetics
Loss of Osteoprotegerin Expression in the Inner Ear Causes Degeneration of the Cochlear Nerve and Sensorineural Hearing Loss
Neurobiology of Disease
Neurology
