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Genetic conditions (Germline genetic disease) Involved chromosomal sites



  • 5q21 is the location of the APC mutation that predisposes for FAP.



  • 11p13 is the site of the WT-1 tumor gene



  • 13q14 is the site of the RB retinoblastoma gene.



  • 17q11 is the site of the NF-1 neurofibromatosis gene,



  • 22q12 is the site of the NF-2 neurofibromatosis gene.

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