OMIA 001300-93934 : Hereditary multiple malformation in Coturnix japonica

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal recessive

Considered a defect: yes

Key variant known: no


1998 Tsudzuki, M., Nakane, Y., Wada, A. :
Hereditary multiple malformation in Japanese quail - a possible powerful animal model for morphogenetic studies Journal of Heredity 89:24-31, 1998. Pubmed reference: 9487677.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005
  • Changed by Frank Nicholas on 15 May 2020