OMIA:001300-93934 : Hereditary multiple malformation in Coturnix japonica (Japanese quail) |
Categories: Mortality / aging (incl. embryonic lethal)
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Disease-related: yes
Key variant known: no
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2020). OMIA:001300-93934: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
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