The detail information of Heterochromia
OMIA Basic Information
Possible human homologues (MIM numbers): -
Mendelian trait/disorder: unknown
Mode of inheritance: -
Considered a defect: yes
Year key mutation first reported: -
Species-specific name: -
Species-specific symbol: -
More detail information can see in
Associated Breeds
There are associated breeds.
Associated Gene
There are no associated genes.
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
| 1959 |
Barone,R.,Lescure,F.: :
[Heterochromia and microphthalmia in the dog] Review Medicine Veterinaire 110:769-792, 1959. |