Specialists
Years of experience in genetics, laboratory diagnostics and bioinformatics
All services
ПГТ-М
MoreПереанализ данных экзома
Срок исследования 14 рабочих дней
12 000 ₽
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Переанализ данных генома
Срок исследования 14 рабочих дней
22 000 ₽
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Non–invasive Prenatal Screening
Исследование ДНК плода по венозной крови матери с целью определения риска возникновения основных синдромов.
MoreFree delivery across Russia
from 17 000 ₽
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All NIPT tests: free genetic counselling in the case of a high-risk result
First Test 21Detects the risk of 1 syndrome
- Down syndrome
- Edwards syndrome
- Patau syndrome
- Turner syndrome
- Trisomy-X
- Klinefelter syndrome
- Jacobs syndrome (disomy - Y)
- XXYY syndrome
- Gender determination (optional)
- Free invasive diagnostics in the case of a high-risk result
- In case of a double pregnancy
Available on credit
First Test LightDetects the risk of 3 syndromes
- Down syndrome
- Edwards syndrome
- Patau syndrome
- Turner syndrome
- Trisomy-X
- Klinefelter syndrome
- Jacobs syndrome (disomy - Y)
- XXYY syndrome
- Gender determination (optional)
- Free invasive diagnostics in the case of a high-risk result
- In case of a double pregnancy
Available on credit
First Test MediumDetects the risk of 6 syndromes
- Down syndrome
- Edwards syndrome
- Patau syndrome
- Turner syndrome
- Trisomy-X
- Klinefelter syndrome
- Jacobs syndrome (disomy - Y)
- XXYY syndrome
- Gender determination (optional)
- Free invasive diagnostics in the case of a high-risk result
- In case of a double pregnancy
Available on credit
First Test Detects the risk of 8 syndromes
- Down syndrome
- Edwards syndrome
- Patau syndrome
- Turner syndrome
- Trisomy-X
- Klinefelter syndrome
- Jacobs syndrome (disomy - Y)
- XXYY syndrome
- Gender determination (optional)
- Free invasive diagnostics in the case of a high-risk result
- In case of a double pregnancy
Available on credit
Free delivery across Russia
30 000 ₽
Mitochondrial genome sequencing
The test is conducted within 75 working days
Chromosomal microarray analysis (CMA)
Срок исследования 35 раб. дней
Progressive Duchenne/Becker muscular dystrophy
A test to confirm the diagnosis of progressive muscular dystrophy and clarify the type of the disease.
MoreIn case of a non-developing pregnancy
Loss of pregnancy is often associated with chromosomal abnormalities in the embryo. Research identifies these abnormalities and helps prepare for your next pregnancy.
MoreSanger sequencing
The most accurate method of determining the nucleotide sequence of the researched area of DNA.
MoreSpinal muscular atrophy (SMA)
A test to confirm the diagnosis of spinal muscular atrophy and clarify the type of disease.
MorePGT-A
Embryo screening during IVF to increase the chances of successful implantation, pregnancy and birth.
MoreGenome sequencing
Examination of genetic damage throughout the DNA sequence in order to find the cause of disease.
MorePaternity Test
A test to determine whether a person is a biological parent with 99.9% accuracy.
MoreExome sequencing
Examination of genetic damage in protein-coding areas of DNA in order to find the cause of disease.
MoreCounselling
For pregnancy planning, suspected inherited diseases and interpretation of genetic tests.
MoreFree delivery across Russia
from 1500 ₽
Laboratory First Genetics
Confidentiality
All data is strictly confidential and cannot be passed on to third parties
Timeframe
Results ready in a short time
Security
Extensive control at each stage of testing
Free delivery
Free delivery of biomaterial across Russia
Charities
Email info@f-genetics.com for information