An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfecta

Journal of Medical Genetics

Volumn 41, Issue 6, 2004, Pages 468-473

  Michaelides, M ^a,b   Bloch Zupan, A ^c,d   Holder, G E ^b   Hunt, D M ^a   Moore, A T ^a,b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b MOORFIELDS EYE HOSPITAL   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d GREAT ORMOND STREET HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMELOGENESIS IMPERFECTA; ARTICLE; COLOR BLINDNESS; DNA EXTRACTION; ENAMEL; FEMALE; GENE MAPPING; GENE MUTATION; GENETIC TRANSCRIPTION; GENOTYPE; HUMAN; MALE; NIGHT VISION; NYSTAGMUS; PHENOTYPE; PHOTOPHOBIA; PHOTORECEPTOR; PRIORITY JOURNAL; RETINA CONE ROD DYSTROPHY; RETINA DISEASE; VISION;

EID: 2942731424     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2003.015792     Document Type: Article

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