CottonR.G.H.: Current methods of mutation detection.Mutat. Res.285: 125–144, 1993.
6.
FriedlW., MeuschelS., CaspariR., LambertiC., KriegerS., SengtellerM., ProppingP.: Attenuated adenomatous polyposis due to a mutation in the 3’ part of the APC gene. A clue for understanding the function of the APC protein.Hum. Genet.,97: 579–584; 1996.
7.
GrodenJ., ThliverisA., SamowitzW., CarlsonM., GelbertL., AlbertsenH., JoslynG., StevensJ., SpirioL., RobertsonM., SargeantL., KrapchoK., WolffE., BurtR., HughesJ.P., WarringtonJ., McPhersonJ., WasmuthJ., Le PaslierD., Abder-rahimH., CohenD., LeppertM., WhiteR.: Identification and characterization of the familial adenomatous polyposis coli gene.Cell, 66: 589–600, 1991.
8.
GrompeM.: The rapid detection of unknown mutations in nucleic acids.Nat. Genet.,5: 111, 1993.
9.
LandegrenU. (ed.): Laboratory protocols for mutation detection.Oxford University Press, Oxford, 1996.
10.
MandlM., KadmonM., SengtellerM., CaspariR., ProppingP., FriedlW.: A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells: implications for predictive diagnosis.Hum. Mol. Genet., 3: 1009–1011, 1994.
11.
NishishoI., NakamuraY., MiyoshiY., MikiY., AndoH., HoriiA., KoyamaK., UtsunomiyaJ., BabaS., HedgeP., MarkhamA., KrushA.J., PetersenG., HamiltonS.R., NilbertM.C., LevyD.B., BryanT.M., PreisingerA.C., SmithK.J., SuL., KinzlerK.W., VogelsteinB.: Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients.Science, 253: 665–669, 1991.
12.
PalmirottaR., CuriaM.C., EspositoD.L., ValanzanoR., MesseriniL., FicariF., BrandiM.L., TonelliF., Mariani-CostantiniR., BattistaP., CamaA.: Novel mutations and inactivation of both alleles of the APC gene in desmoid tumors.Hum. Mol. Genet., 4: 1979–1981, 1995.
RoestP.A., RobertsR.G., SuginoS., van OmmenG.J., den Dun-nenJ.T.: Protein truncation test (PTT) for rapid detection of translation-terminating mutations.Hum. Mol. Genet., 2: 1719–1721, 1993.
17.
van der LuijtR.B., VasenH.F.A., TopsC.M.J., BreukelC., FoddeR., Meera KhanP.: APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis.Hum. Genet., 96: 705–710, 1995.
18.
VarescoL., GrodenJ., SpirioL., RobertsonM., WeissR., GismondiV., FerraraG.B., WhiteR.: A rapid screening method to detect nonsense and frameshift mutations: identification of disease-causing APC alleles.Cancer Res., 53: 5581–5584, 1993.
19.
VarescoL., GismondiV., PresciuttiniS., GrodenJ., SpirioL., SalaP., RossettiC., De BenedettiL., BaficoA., HeouaineA., GrammaticoP., Del PortoG., WhiteR., BertarioL., FerraraG.B.: Mutation in a splice-donor site of the APC gene in a family with polyposis and late age of colonic cancer of death.Hum. Genet., 93: 281–286, 1994.