The ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic retinitis pigmentosa

Ophthalmic Genetics

Volumn 18, Issue 1, 1997, Pages 13-26

  Iannaccone, A ^a   De Propris, G ^a   Roncati, S ^a   Rispoli, E ^a   Del Porto, G ^a   Pannarale, M R ^a  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

Bardet Biedl syndrome; Genotype; Optic atrophy; Phenotype; Psychophysics; Retinitis pigmentosa

Indexed keywords

VISUAL PIGMENT;

ADOLESCENT; ADULT; ARTICLE; BARDET BIEDL SYNDROME; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL FEATURE; COLOR VISION; CONTROLLED STUDY; ELECTRORETINOGRAPHY; EYE FUNDUS; EYE MOVEMENT; FEMALE; HUMAN; MALE; NYSTAGMUS; OPTIC DISK; OPTIC NERVE ATROPHY; PHENOTYPE; PRIORITY JOURNAL; RETINA MACULA LUTEA; RETINITIS PIGMENTOSA; SCHOOL CHILD; STRABISMUS; VISUAL ACUITY;

EID: 0030967419     PISSN: 01676784     EISSN: None     Source Type: Journal    
DOI: 10.3109/13816819709057879     Document Type: Article

References (57)