Анализдер

Барлық анализдер

Тексерулер

Determination of genetic causes of azoospermia (AZF locus - locus deletions)

430 000 Сум

DNA fragmentation of sperm

1 400 000 Сум

Thrombophilia, genetic predisposition (F2, F5, F7, F13A1, FGB, PAI-1, ITGA2-a2, ITGB3-b3 gene mutations)

1 480 000 Сум

Parentage determination (2 subjects)

1 940 000 Сум

Neonatal screening of newborns for amino acids and acylcarnitines

400 000 Сум

Epstein Barr virus (PCR)

350 000 Сум

Metabolism, weight correction (PPFRG2,ADRB2, ADRB3, FABP2)

1 530 000 Сум

Comprehensive genomic profiling of tumors (tissue)

29 870 000 Сум

Whole genome sequencing with clinical interpretation (cWGS)

19 845 000 Сум

Carrier screening for hereditary diseases (extended panel)

4 850 000 Сум

Oncopanel “Hereditary colorectal cancer”.

4 850 000 Сум

Whole exome sequencing with clinical interpretation (WES)

10 925 000 Сум

Urgent Whole Exome Sequencing with Clinical Interpretation (citoWES)

13 805 000 Сум

Oncopanel “Hereditary prostate cancer”.

4 850 000 Сум

Diagnosis of Fragile X syndrome (Fragile X)

2 975 000 Сум

Karyotyping (Cytogenetics)

1 180 000 Сум

Hemophilia A Diagnosis

2 975 000 Сум

Female Oncology Panel

5 950 000 Сум

Comprehensive genomic profiling of tumors (blood)

59 740 000 Сум

Hereditary Breast and Ovarian Cancer Oncopanel

4 850 000 Сум
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