[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]
No abstract available

MeSH terms

  • Albinism*
  • Amblyopia*
  • Astigmatism*
  • Chromosome Aberrations*
  • Color Vision Defects*
  • Eye Diseases*
  • Fundus Oculi*
  • Humans
  • Macula Lutea*
  • Myopia*
  • Nystagmus, Pathologic*