OMIA:000783-9685 : Pelger-Huet anomaly in Felis catus (domestic cat) |
In other species: dog , rabbit
Categories: Haematopoietic system phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 169400 (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:000783-9685: 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.
| 2003 | Oosterwijk, J.C., Mansour, S., van Noort, G., Waterham, H.R., Hall, C.M., Hennekam, R.C. : |
| Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes. J Med Genet 40:937-41, 2003. Pubmed reference: 14684694. | |
| 1988 | Latimer, K.S., Rowland, G.N., Mahaffey, M.B. : |
| Homozygous Pelger-Huët anomaly and chondrodysplasia in a stillborn kitten Vet Pathol 25:325-8, 1988. Pubmed reference: 3407106. | |
| 1985 | Latimer, K.S., Rakich, P.M., Thompson, D.F. : |
| Pelger-Huët anomaly in cats. Vet Pathol 22:370-4, 1985. Pubmed reference: 4035941. DOI: 10.1177/030098588502200412. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005