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Intra-familial phenotype variability in patients with Jalili syndrome

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Bibliographic Details
Published in:	Eye (London) 2015-05, Vol.29 (5), p.712-716
Main Authors:	Gerth-Kahlert, C, Seebauer, B, Dold, S, Hanson, J V M, Wildberger, H, Spörri, A, van Waes, H, Berger, W
Format:	Article
Language:	English
Subjects:	45/23 692/1807/1482 692/308/409 692/699/3161/3165 Adolescent Amelogenesis Imperfecta - genetics Amelogenesis Imperfecta - pathology Cation Transport Proteins - genetics Correspondence DNA Mutational Analysis Electroretinography Genetic Variation Humans Laboratory Medicine Medicine Medicine & Public Health Mutation Ophthalmology Pharmaceutical Sciences/Technology Phenotype Retina - pathology Retinitis Pigmentosa - genetics Retinitis Pigmentosa - pathology Siblings Surgery Surgical Oncology Tomography, Optical Coherence
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