Presymptomatic direct detection of adenomatous polyposis coli (APC) gene mutations in familial adenomatous polyposis
- 1 May 1993
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 91 (4) , 307-311
- https://doi.org/10.1007/bf00217347
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Molecular analysis of APC mutations in familial adenomatous polyposis and sporadic colon carcinomasThe Lancet, 1992
- Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresisGenomics, 1992
- Familial adenomatous polyposis: Identification of a new frameshift mutation of the APC gene in an Italian familyBiochemical and Biophysical Research Communications, 1992
- Predictive diagnosis of familial adenomatous polyposis with linked DNA markers: population based study.BMJ, 1992
- Identification of FAP Locus Genes from Chromosome 5q21Science, 1991
- Identification and characterization of the familial adenomatous polyposis coli geneCell, 1991
- The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations.Journal of Medical Genetics, 1991
- Mutation Analysis for Heterozygote Detection and the Prenatal Diagnosis of Cystic FibrosisNew England Journal of Medicine, 1990
- ANTENATAL DIAGNOSIS OF SICKLE-CELL ANÆMIA BY D.N.A. ANALYSIS OF AMNIOTIC-FLUID CELLSThe Lancet, 1978
- Penetrance and expressivity of the gene responsible for the Gardner syndromeClinical Genetics, 1977