The detail information of Osteogenesis imperfecta, generic
OMIA Basic Information

Possible human homologues (MIM numbers):

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal Dominant

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.
2000 Lazar,T.,deHaan,J.J.,Peck,J.N.,Campbell,B.G.,Ginn,P.E.,Phillips,L.,Suero,A.,Chase,J.: :
Osteogenesis imperfecta in three dogs from a single litter Veterinary & Comparative Orthopaedics & Traumatology 13:23-27, 2000.
1997 Campbell,B.G.,Wootton,J.A.M.,Krook,L.,Demarco,J.A.,Minor,R.R.: :
Clinical signs and diagnosis of osteogenesis imperfecta in three dogs Journal of the American Veterinary Medical Association 211:183 ff., 1997.
Pubmed reference: 9227748 .
1991 Konig,F.: :
Case Report - Osteogenesis Imperfecta in a German Shepherd Puppy Kleintierpraxis 36:583, 1991.
1960 Lettow,E.,Dammrich,K.: :
[Contribution to the clinical picture and pathology of Osteogenesis imperfecta in the young dog.] Beitrag zur Klinik und Pathologie der Osteogenesis imperfecta bei Junghunden. Zentralblatt fur Veterinarmedizin 7:936-966, 1960.
1956 Calkins,E.,Kalm,D.,Diner,W.C.: :
Idiopathic familial osteoporosis in dogs: 'Osteogenesis imperfecta' Annals of the New York Academy of Sciences 64:410-423, 1956.