No abstract available
MeSH terms
-
Blindness / diagnosis*
-
Blindness / embryology
-
Embryo, Mammalian / pathology
-
Female
-
Fetal Diseases / pathology
-
Humans
-
Immunohistochemistry
-
Mutation
-
Optic Atrophy, Hereditary, Leber / diagnosis*
-
Optic Atrophy, Hereditary, Leber / embryology
-
Optic Atrophy, Hereditary, Leber / genetics
-
Optic Atrophy, Hereditary, Leber / pathology
-
Pedigree
-
Prenatal Diagnosis*
-
Retina / embryology
-
Retinal Degeneration / diagnosis*
-
Retinal Degeneration / embryology