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].


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