Nomenclature for inherited diseases of the retina [5]

American Journal of Human Genetics

Volumn 58, Issue 2, 1996, Pages 433-436

  Inglehearn, C F ^a   Hardcastle, A J ^a   Daiger, S P ^a   McGuire, R E ^a   Heckenlively, J R ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

PERIPHERIN; RHODOPSIN;

CHROMOSOME; ELECTRORETINOGRAM; FEMALE; GENE; HAPLOTYPE; HETEROZYGOTE; HUMAN; LETTER; MALE; NOMENCLATURE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; RETINA DEGENERATION; RETINOPATHY; X CHROMOSOME INACTIVATION; X CHROMOSOME LINKED DISORDER;

CHROMOSOME MAPPING; FEMALE; GENES, DOMINANT; GENES, RECESSIVE; HUMANS; MALE; PHENOTYPE; RETINAL DEGENERATION; RETINITIS PIGMENTOSA; TERMINOLOGY; X CHROMOSOME;

EID: 0030070409     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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