Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes

J Med Genet. 2003 Dec;40(12):937-41. doi: 10.1136/jmg.40.12.937.
No abstract available

Publication types

  • Comparative Study
  • Letter
  • Review

MeSH terms

  • Abnormalities, Multiple / diagnosis*
  • Abnormalities, Multiple / genetics
  • Alleles
  • Animals
  • Bone Diseases, Developmental / congenital*
  • Bone Diseases, Developmental / diagnosis*
  • Bone Diseases, Developmental / genetics
  • Calcinosis / congenital
  • Calcinosis / diagnosis
  • Calcinosis / genetics
  • Homozygote
  • Humans
  • Hydrops Fetalis / diagnosis
  • Hydrops Fetalis / genetics
  • Mice
  • Pelger-Huet Anomaly / congenital*
  • Pelger-Huet Anomaly / diagnosis*
  • Pelger-Huet Anomaly / genetics
  • Phenotype
  • Rabbits
  • Survival Analysis
  • Syndrome