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Kalıtsal Kanser
Application Region Art.Nr.
Peutz-Jeghers syndrome (PJS) STK11 19p13.3 P101
Retinoblastoma (RB) RB1 13q14 P047
Rhabdoid tumors SMARCB1 22q11.2 P258
Tumours, Cutaneous melanoma 9p21, CDKN2A, CDKNA2B ME024
Von Hippel-Lindau Syndrome VHL, 3p25 P016
Wilms tumours, WAGR, Denys-Drash, Frasier syndrome. WT1 11p13 P118
Ataxia-Telangiectasia (AT) ATM 11q23 P041
Ataxia-Telangiectasia (AT) ATM 11q23 P042
Breast cancer susceptibility CHEK2 22q12, ATM , PTEN, TP53 P190
Breast cancer, hereditary BRCA2, CHEK2 P045
Breast cancer, hereditary BRCA2 P077
Breast cancer, hereditary BRCA1 P087
Breast cancer, hereditary BRCA2 13q12.3 P090
Breast cancer BRCA1 region P239
CDH1 or E-cadherin CDH1 16q22.1 P083
Cancer PTEN 10q23 P225
Cancer BRIP1 17q22, CHEK1 11q22 P240
Colon cancer, hereditary non-polyposis (HNPCC) MLH1 3p21.3, MSH2 2p21 P248
Colon cancer, stomach cancer (hereditary) 1p34 and 15q13 P378
Fanconi Anemia RAD50 P260
Fanconi anemia (FA) FANCD2. 3p25.3, PALB2 16p12 P057
Fanconi anemia complementation group B FANCB Xp22 P113
Gorlin syndrome PTCH 9q22.3 P067
Hereditary Polyposis Colon Cancer APC, 5q21-q22 P043
Hereditary breast cancer 17q21.31 P002
Hereditary nonpolyposis colon cancer (HNPCC) MSH6 P072
Hereditary nonpolyposis colon cancer (HNPCC) MLH1 3p21.3, MSH2 2p22 P003
Hereditary nonpolyposis colon cancer (HNPCC) PMS2 7p22 P008
Juvenile polyposis syndrome (JPS) BMPR1A 10q22, SMAD4 18q21, PTEN P158
Li-Fraumeni syndrome (LFS) P53 17q13.1 P056
Lynch syndrome MHL1, MSH2, CDKN2A, BRAF V600E ME043-basic research
Melanocytic tumours, mesothelioma 3p21.1 P417
Multiple Osteochondromas EXT1 8q24, EXT2 11p12 P215
Neurofibromatosis type 2 (NF2) NF2 22q12 P044
Neurofibromatosis NF1 17q11.2 P081
Neurofibromatosis NF1 17q11.2 P082
Neurofibromatosis NF1 17q11.2 P122
Paragangliomas (PGL) SDHD 11q23.1, SDHB 1p36.1, SDHC 1q23.3 P226

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