Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1992-5-1
pubmed:abstractText
In short-term cultures of tumor tissue from a medullary thyroid carcinoma (MTC), we found a large clone of cells with a balanced translocation t(9;12)(p24;q22). A large clone with a balanced translocation t(10;16)(p11;q24) was also found in cultures from a C-cell thyroid hyperplasia. No clearcut evidence for chromosome instability was observed in the lymphocytes of the two patients. The mother of the first patient died of MTC; two relatives of the second patient had MTC and one of them had pheochromocytoma. These findings classify the two subjects as MEN 2A patients with different phenotypic expression but with the same type of chromosomal abnormality.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0165-4608
pubmed:author
pubmed:issnType
Print
pubmed:volume
59
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
51-3
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed-meshheading:1348208-Adult, pubmed-meshheading:1348208-Carcinoma, pubmed-meshheading:1348208-Chromosome Aberrations, pubmed-meshheading:1348208-Chromosome Banding, pubmed-meshheading:1348208-Chromosome Deletion, pubmed-meshheading:1348208-Chromosome Disorders, pubmed-meshheading:1348208-Chromosomes, Human, Pair 10, pubmed-meshheading:1348208-Chromosomes, Human, Pair 12, pubmed-meshheading:1348208-Chromosomes, Human, Pair 16, pubmed-meshheading:1348208-Chromosomes, Human, Pair 9, pubmed-meshheading:1348208-Female, pubmed-meshheading:1348208-Humans, pubmed-meshheading:1348208-Hyperplasia, pubmed-meshheading:1348208-Karyotyping, pubmed-meshheading:1348208-Male, pubmed-meshheading:1348208-Multiple Endocrine Neoplasia, pubmed-meshheading:1348208-Thyroid Gland, pubmed-meshheading:1348208-Translocation, Genetic
pubmed:year
1992
pubmed:articleTitle
Cytogenetics of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasia.
pubmed:affiliation
Biologia Generale e Genetica Medica, Università di Pavia, Italy.
pubmed:publicationType
Journal Article, Case Reports