Nomenclature for inherited diseases of the retina

Am J Hum Genet. 1996 Feb;58(2):433-5.

Authors

C F Inglehearn, A J Hardcastle

PMID: 8571973
PMCID: PMC1914532

No abstract available

Publication types

Comment
Letter

MeSH terms

Chromosome Mapping
Female
Genes, Dominant / genetics
Genes, Recessive
Humans
Male
Phenotype
Retinal Degeneration / genetics*
Retinitis Pigmentosa / genetics*
Terminology as Topic*
X Chromosome