OMIA 000783-9685 : Pelger-Huet anomaly in Felis catus |
In other species:
dog
,
rabbit
Possibly relevant human trait(s) and/or gene(s) (MIM number):
169400 (trait)
Mendelian trait/disorder:
unknown
Considered a defect:
yes
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. : | |
| Vet Pathol 22:370-4, 1985. Pubmed reference: 4035941. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005