OMIA:000783-9685 : Pelger-Huet anomaly in Felis catus (domestic cat)
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
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
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.|
- Created by Frank Nicholas on 06 Sep 2005