A homozygous mutation in MSH6 causes Turcot syndrome. [electronic resource]
Producer: 20051207Description: 4689-93 p. digitalISSN:- 1078-0432
- Adenomatous Polyposis Coli -- genetics
- Base Sequence
- Brain Neoplasms -- genetics
- Child
- Chromatography, High Pressure Liquid -- methods
- DNA Mutational Analysis
- DNA-Binding Proteins -- genetics
- Family Health
- Female
- Glial Fibrillary Acidic Protein -- analysis
- Homozygote
- Humans
- Immunohistochemistry
- Ki-67 Antigen -- analysis
- Male
- Microsatellite Repeats -- genetics
- Mutagenesis, Insertional
- Mutation
- Pedigree
- Sequence Homology, Nucleic Acid
- Syndrome
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Publication Type: Case Reports; Journal Article
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