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Volumn 38, Issue 10, 2001, Pages
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The Asp1822Val variant of the APC gene is a common polymorphism without clinical implications.
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Author keywords
[No Author keywords available]
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Indexed keywords
ALLELE;
CAUCASIAN;
COLORECTAL TUMOR;
GENETIC POLYMORPHISM;
GENETIC PREDISPOSITION;
GENETIC SCREENING;
GENETIC VARIABILITY;
GENETICS;
HETEROZYGOTE;
HOMOZYGOTE;
HUMAN;
LETTER;
MISSENSE MUTATION;
NUCLEOTIDE SEQUENCE;
PHENOTYPE;
REPRODUCIBILITY;
SPAIN;
TUMOR SUPPRESSOR GENE;
ALLELES;
COLORECTAL NEOPLASMS;
DNA MUTATIONAL ANALYSIS;
EUROPEAN CONTINENTAL ANCESTRY GROUP;
GENES, APC;
GENETIC PREDISPOSITION TO DISEASE;
GENETIC SCREENING;
HETEROZYGOTE;
HOMOZYGOTE;
HUMANS;
MUTATION, MISSENSE;
PHENOTYPE;
POLYMORPHISM, GENETIC;
REPRODUCIBILITY OF RESULTS;
SPAIN;
VARIATION (GENETICS);
MLCS;
MLOWN;
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EID: 0035487312
PISSN: None
EISSN: 14686244
Source Type: Journal
DOI: 10.1136/jmg.38.10.e33 Document Type: Letter |
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Times cited : (18)
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References (0)
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