[A NEW EYE SYNDROME WITH X-CHROMOSOMAL TRANSMISSION. A FAMILY CLAN WITH FUNDUS ALBINISM, FOVEA HYPOPLASIA, NYSTAGMUS, MYOPIA, ASTIGMATISM AND DYSCHROMATOPSIA]
Klin Monbl Augenheilkd
.
1964 Apr:144:447-57.
[Article in German]
Authors
H FORSIUS
,
A W ERIKSSON
PMID:
14230113
No abstract available
MeSH terms
Albinism*
Amblyopia*
Astigmatism*
Chromosome Aberrations*
Color Vision Defects*
Eye Diseases*
Fundus Oculi*
Humans
Macula Lutea*
Myopia*
Nystagmus, Pathologic*