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Genetic laboratory tests

40.00 1,950.00 

x 30 Min(s)


Choose a date above to see available times.

New technologies of genetic testing make it possible to diagnose complex diseases and choose the most appropriate treatment method. At the Socrates clinic, we offer non-invasive prenatal, family planning, rare hereditary diseases and other tests. Family planning studies, suitable for those planning and preparing for pregnancy or expecting a baby, accurately show potential risks. With high-risk results, other targeted tests can be done to see if the baby has a genetic disease. Family planning studies help to properly plan a pregnancy, prepare for child care, and make reasonable family planning decisions. During pregnancy, we offer an early genetic test from the 10th week onwards – it is a non-invasive prenatal test (NIPT), which particularly accurately assesses the risk of the unborn fetus for the most common genetic diseases from the fetal DNA in the mother’s blood. Conducted research helps identify rare and undiagnosed diseases – this allows better prediction of the course of the disease and prevention of complications.

Genetic lab tests

Additional study father, Additional study relative, Ancestral genealogy map – 1 person being studied (father's line of descent), Ancestral Origins – map and report e-mail by post, Ancestry map – 1 person being studied (mother's line of descent), Ancestryby DNA certificate term, Comparison of the new DNA profile with those already available in the laboratory, Court expert opinion, DNA Non-Invasive Prenatal Paternity Test (Additional Putative Father), DNA Non-invasive prenatal paternity test (where the expectant mother and putative father are tested), DNA profile comparison from document (DNA profile), DNA profile test – 1 person, DNA profile test – 2 persons, DNA study of the child's personality – 2 children are studied, DNA test for determining the sex of the fetus (from the 9th week of pregnancy), DNA test of child's personality – 1 child is tested, DNA test of consanguinity when 3 presumed relatives are tested, DNA test of consanguinity when testing 2 presumed relatives, DNA test of genetic predisposition to diseases – 1 person, DNA test response transcript (from archive), DNA testing for genetic reconstruction, DNAFIT DIET, DNAfit DIET supplement. 3-month NUTRITION PLAN with menu, Examination of an additional DNA sample from saliva (with the help of an applicator), Examination of an additional sperm sample from tissue (clothing) by extracting DNA, Examination of sperm from tissue (clothing) by extracting DNA, Examination of sperm from tissue (clothing) by extracting DNA + 1 comparative DNA sample from saliva (with the help of an applicator), Express service within 5 days. d. (Determining the sex of the fetus), Family planning study (1 subject + genetic risk analysis for partner) CentoScreen Paired, Family Planning Study (1 Subject) CentoScreen SOLO, Family Planning Study (Subject 2) CentoScreen DUO, Grandparents DNA test (both grandparents and 1 child are tested), Grandparents DNA test (both grandparents and 2 children are tested), Grandparents DNA test (both grandparents, mother and 1 child are tested), Inbreeding DNA test where 4 presumed relatives are tested, Large map (69 x 43 cm) by post, Maternal DNA test – 1 mother and 1 child are tested, Maternal DNA test – 1 mother and 2 children are tested, Maternal DNA test – 1 mother and 3 children are tested, mtDNA Test – 2 persons, mtDNA Test – 3 persons, NIPT Serenity + microdeletion + whole chromosome test, NIPT Serenity + microdeletion assay, NIPT Serenity + Whole Chromosome Test, NIPT Serenity Baseline Study, Paternity test – the alleged father and 1 child are tested, Paternity test – the alleged father and 2 children are tested, Paternity test – the alleged father and 3 children are tested, Paternity test – the alleged father, mother and 1 child are tested, Paternity test – the alleged father, mother and 2 children are tested, Paternity test – the alleged father, mother and 3 children are tested, Prenatal examination Cento NIPT, Prenatal examination NIPT Invitae, Prenatal Harmony study + detection of Di George (22q11.2) microdeletion, Prenatal Harmony Test (NIPT), Priority service within 8 days. d. (Determining the sex of the fetus), Refusal of DNA testing when DNA samples have already been taken (administrative fee), Sperm detection on tissue (sperm protein is detected. DNA is not extracted), Standard size map (43 x 27 cm) by mail, Uncle/aunt DNA test (1 aunt/uncle and 1 child (2 persons) are tested, Uncle/Aunt DNA test (1 aunt/uncle and 2 children (3 individuals) are tested, Uncle/Aunt DNA test (testing 1 aunt/uncle and mother and 1 child (3 persons), Uncle/Aunt DNA test (tests 1 aunt/uncle and mother and 2 children (4 persons), X-Chromosome Test – 2 persons, X-Chromosome Test – 3 persons, Y-Chromosome Test – 2 persons, Y-Chromosome Test – 3 persons

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