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Phenotype in 18 Danish subjects with genetically verified CHARGE syndrome
E Husu,
Hanne Buciek Hove
, S Farholt, M Bille,
L Tranebjaerg
, Ida Vogel,
S Kreiborg
Department of Clinical Genetics
Department of Otorhinolaryngology, Head and Neck Surgery and Audiology
Department of Dental, Oral and Maxilliofacial Surgery
37
Citations (Scopus)
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Nursing and Health Professions
DNA Binding Protein
100%
Syndrome CHARGE
100%
Helicase
100%
Nuclear Magnetic Resonance Imaging
66%
Choana atresia
66%
Ear Malformation
66%
Coloboma
66%
Economic and Social Development
66%
Medical Record
33%
Syndrome
33%
Prevalence
33%
Clinical Feature
33%
Computer Assisted Tomography
33%
Hearing Impairment
33%
Neonate
33%
Perception Deafness
33%
Genetic Screening
33%
Three Dimensional Imaging
33%
Multiple Malformation Syndrome
33%
Hypoplasia
33%
Vestibular Disorder
33%
Biochemistry, Genetics and Molecular Biology
Helicase
100%
Chromodomain
100%
DNA-binding Protein
100%
Growth, Development and Aging
66%
Magnetic Resonance Imaging
66%
Hearing
66%
Genetics
33%
Prevalence
33%
Genetic Screening
33%
Reconstruction
33%
Computer Assisted Tomography
33%
Medical Record
33%
Genotype-Phenotype Correlation
33%
Neuroscience
Helicase
100%
DNA-binding Protein
100%
Magnetic Resonance Imaging
66%
Genetics
66%
Computed Tomography
33%
Hypoplasia
33%
Sensorineural Hearing Loss
33%
Temporal Bone
33%
Cranial Nerve
33%
Keyphrases
Retarded Growth
100%
Medicine and Dentistry
Multiple Abnormalities
33%