homozygosis


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ho·mo·zy·go·sis

 (hō′mō-zī-gō′sĭs, -mə-, hŏm′ə-)
n.
1. Formation of a homozygote, especially by unusual means such as mitotic recombination or gene conversion.
2. The condition of being a homozygote.

ho′mo·zy·got′ic (-gŏt′ĭk) adj.

ho•mo•zy•go•sis

(ˌhoʊ mə zaɪˈgoʊ sɪs, -zɪ-, ˌhɒm ə-)

n.
the state of being a homozygote.
[1900–05]
References in periodicals archive ?
A deep vein thrombosis caused by 20209 C>T mutation in homozygosis of the prothrombin gene in a Caucasian patient.
4 allele in both homozygosis and heterozygosis increases the risk of developing AD.
Diminishing productivity, ability to transform feed into meat, and resistance to environmental conditions and illness, and increasing number of deformations are some of the most important negative effects of decreasing genetic variation as a result of increasing homozygosis (Karahan et al.
Therefore, segregating generations will lead to homozygosis, and it is expected that heterosis will be reduced by half in each self-fertilized generation.
Homozygosis for the MnSOD Val allele contributed to development of DN in Finnish and Swedish patients with type 1 diabetes (73).
The heterozygous state is clinically asymptomatic and its homozygosis is the rarest form of inheritance.
This aspect offer enough space for further implementation of selection program based on homozygosis on LGB gene.