Specialists
Years of experience in genetics, laboratory diagnostics and bioinformatics
Hereditary breast and ovarian cancer syndrome caused by mutations in the BRCA1 or BRCA2 genes.
Hereditary breast cancer caused by mutations in the PALB2 gene.
Familial atypical multiple mole melanoma syndrome (FAMMM) caused by mutations in the p16/CDKN2A gene and associated with melanomas of the skin and eyes.
Familial pancreatitis, usually caused by mutations in the PRSS1 gene.
Lynch syndrome, also known as hereditary non-polyposis colorectal cancer (HNPCC), is most often caused by a defect in the MLH1 or MSH2 genes.
Peutz-Jeghers syndrome caused by defects in the STK11 gene. This syndrome is also associated with polyps in the digestive tract and some other cancers.
Years of experience in genetics, laboratory diagnostics and bioinformatics
All data is strictly confidential and cannot be passed on to third parties
Results ready in a short time
Extensive control at each stage of testing
Free delivery of biomaterial across Russia
Email info@f-genetics.com for information
Шикеева Амуланг Алексеевна
Врач-генетик, лабораторный генетик Лаборатории First Genetics, к.м.н.
Филатов Павел Николаевич
Врач-онколог, химиотерапевт высшей категории, хирург ГАУЗ «ООКСЦТО» Действительный член Российского общества клинической онкологии (RUSSCO), Ассоциации онкологов России (АОР), профессионального сообщества Меланома Про.