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Тесты

Вопрос 
1
A cell of granular endoplasmatic reticulum is at the stage of translation, when mRNA advances to the ribosomes. Amino acids get bound by peptide bonds in a certain sequence thus causing polypeptide biosynthesis. The sequence of amino acids in a polypeptide corresponds with the sequence of:





2
In Western Europe nearly half of all congenital malformations occur in the children conceived in the period, when pesticides were used extensively in the region. Those congenital conditions result from the following influence:





3
In some areas of South Africa many people have sickle cell disease characterized by red blood cells that assume an abnormal sickle shape due to the substitution of glutamic acid for valine in the hemoglobin molecule. What is the cause of this disease?





4
A hospital in Donetsk region admitted the patients - members of the same family - with eyelid and face edemata, fever, eosinophilia, headache, muscle pain. The disease developed on the 7-10 day after eating pork sausage sent by the patients’ relatives from Khmelnitsky region. What is your provisional diagnosis?





5
A woman had been taking synthetic hormones during her pregnancy. Her newborn girl presents with excessive hairiness which has formal resemblance to adrenogenital syndrome. This sign of variability is called:





6
A diet must include fats. Fats perform plastic function in an organism due to their inclusion in:





7
Enamel hypoplasia is caused by a dominant gene localized in the X chromosome. Mother has a normal enamel, and father has enamel hypoplasia. Which of children will have this anomaly?





8
Studying the mitotic cycle phases of an onion root the researchers revealed a cell with chromosomes lying in equatorial plane in form of a star. What phase of mitosis is it?





9
In case of some helminthiases, an affected person can detect helminth himself because mature segments of the causative agent are able to crawl out of the anus. This is typical for the following disease:





10
Human X chromosome contains a dominant gene that is reponsible for normal blood clotting. An autosomal dominant gene plays a similar role. Lack of any of these genes leads to the coagulation disorder. The form of interaction between these genes is called:





 
 
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