OMIA:000783-9685 : Pelger-Huet anomaly in Felis catus (domestic cat)

In other species: dog , rabbit

Categories: Haematopoietic system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 169400 (trait)

Mendelian trait/disorder: unknown

Considered a defect: yes

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000783-9685: 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.

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