Home » gene table » Cartera de servicios cancer familiar

CHECK HERE OUR PORTFOLIO OF NGS SERVICES FOR GENETIC DIAGNOSIS IN FAMILIAL CANCER

Reference

Disease

SEQ1637 Fanconi anemia
SEQ1065 Familial Colorectal Cancer
SEQ1067 Familial Endometrial Cancer
SEQ1357 Bone and Soft Tissue Cancer (Sarcoma and Osteosarcoma)
SEQ1052 Familial breast / ovarian cancer
SEQ1070 Ovarian Cancer
SEQ1358 Hereditary skin cancer
SEQ1055 Familial Prostate Cancer
SEQ1355 Central nervous system cancer
SEQ1354 Cancer of the nervous / brain system (glioma)
SEQ1069 Extended Familial Endocrine Cancer
SEQ1053 Familial gastric cancer
SEQ1066 Familial Pancreatic Cancer
SEQ1058 Familial Parathyroid Cancer
SEQ1054 Familial kidney cancer
SEQ1057 Familial Thyroid Cancer
SEQ1345 Familial non-medullary thyroid cancer
SEQ1064 Familial Chondrosarcoma
EXN1040/SEQ1350 Congenital Blackfan-Diamond Erythorblastopenia and Differential Diagnosis
SEQ1060 Familial Pheochromocytoma
SEQ1063 Familial Melanoma
SEQ1056 Familial Multiple Endocrine Neoplasia
SEQ1081 FAMILIAL BREAST/OVARIAN CANCER
SEQ1343 Familial adenomatous polyposis
SEQ1344 Juvenile polyposis
SEQ1348 Predisposition to pediatric hematitis
EXN1149/SEQ1347 Predisposition to myeloid pathologies
SEQ1359 Predisposition to pediatric solid tumors
SEQ1360 Predisposition to expanded cancer, multiple types
SEQ1049 Predisposition to cancer, multiple types
EXN1120/SEQ1349 Hereditary syndromes with bone marrow failure
SEQ1346 Wilms tumor
SEQ references correspond to studies performed using NIMSeq®
EXN references correspond to studies performed using ExoNIM®

To consult the genes associated with each approach and the complete catalog of services, go to our genetics test search tool

Genetic test search