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1.
Lik Sprava ; (7): 15-21, 2013.
Artigo em Russo | MEDLINE | ID: mdl-25509909

RESUMO

Moderate doses of radiation exposure in the early period of embryogenesis may become the reason of occurrence of uterus duplex and raise a follicular unit ovarian the future girl of that predetermines a high probability of malformations of the fetus during future pregnancies after reaching adult age.


Assuntos
Desenvolvimento Fetal , Feto/anormalidades , Complicações na Gravidez/etiologia , Útero/anormalidades , Aborto Induzido , Adulto , Feminino , Humanos , Gravidez , Complicações na Gravidez/diagnóstico por imagem , Complicações na Gravidez/genética , Ultrassonografia
2.
Tsitol Genet ; 39(4): 41-4, 2005.
Artigo em Russo | MEDLINE | ID: mdl-16396330

RESUMO

As it is universally recognized, the population is a sound criteria of the environment quality. The most reliable method to evaluate genetic processes in a population under the condition of the environmental pollution is genetic monitoring, a survey of dynamic parameters of genetic load. An evaluation of genetical safety of an urbanized area of a city is represented in this article. The parameters of genetic load like congenital malformations and multifactorial diseases have been used in the models of monitoring. The analysis and comparison of disease frequencies in Kharkiv Dzerzhinsky District, in other European populations and in regional rural districts with various levels of production have been made.


Assuntos
Doenças Genéticas Inatas/epidemiologia , Predisposição Genética para Doença/epidemiologia , Testes Genéticos , População Urbana , Adolescente , Criança , Pré-Escolar , Doenças Genéticas Inatas/genética , Humanos , Lactente , Recém-Nascido , População Rural , Ucrânia/epidemiologia
3.
Tsitol Genet ; 35(1): 74-8, 2001.
Artigo em Russo | MEDLINE | ID: mdl-11589049

RESUMO

By means of genetic analysis of 400 individuals suffering from psoriasis the mendelian inheritance model have been rejected: the segregation frequencies are SFNxN = 0.083 and SFNxA = 0.1474. The heritability of psoriasis in the polygenic model is about 100%. The main gene model with incomplete penetration have been proposed (p = 0.044, [symbol: see text]1 = 6.1%, [symbol: see text]2 = 82.2%). 0.189% residents of Kharkov population are homozygotes and 8.32% heterozygotes on psoriatic gene, 0.155% residents are suffering from psoriasis heterozygotes and 0.508% heterozygotes. Among individuals suffering from psoriasis 23% are homozygotes and 77% heterozygotes.


Assuntos
Frequência do Gene , Psoríase/genética , Genótipo , Heterozigoto , Homozigoto , Humanos , Masculino , Modelos Genéticos , Herança Multifatorial , Linhagem , Penetrância , Psoríase/epidemiologia , Ucrânia/epidemiologia
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