OMIA:001168-9986 : Coronal suture synostosis in Oryctolagus cuniculus (rabbit) |
Categories: Skeleton phene (incl. short stature & teeth)
Possibly relevant human trait(s) and/or gene(s) (MIM number): 123100 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Genetic engineering:
Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:001168-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
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.
| 1996 | Smith, T.D., Mooney, M.P., Burrows, A.M., Losken, H.W., Siegel, M.I. : |
| Postnatal changes in the cranial base in rabbits with congenital coronal suture synostosis Journal of Craniofacial Genetics & Developmental Biology 16:107-117, 1996. | |
| 1995 | Burrows, A.M., Mooney, M.P., Smith, T.D., Losken, H.W., Siegel, M.I. : |
| Growth of the cranial vault in rabbits with congenital coronal suture synostosis Cleft Palate - Craniofacial Journal 32:235-246, 1995. Pubmed reference: 7605791. DOI: 10.1597/1545-1569(1995)032<0235:GOTCVI>2.3.CO;2. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005