A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors. [electronic resource]
Producer: 19981223Description: 1544-9 p. digitalISSN:- 0002-9297
- Adolescent
- Adult
- Aged
- Amino Acid Substitution
- Calcium -- blood
- Child
- Chromosome Mapping
- Chromosomes, Human, Pair 11
- Female
- Genes, Dominant
- Humans
- Hyperparathyroidism -- genetics
- Loss of Heterozygosity
- Male
- Middle Aged
- Mutation, Missense
- Neoplasm Proteins -- genetics
- Parathyroid Neoplasms -- genetics
- Pedigree
- Proto-Oncogene Proteins
No physical items for this record
Publication Type: Letter; Research Support, Non-U.S. Gov't
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