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Volumn 131, Issue 5, 2002, Pages 509-514
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V804M RET mutation and familial medullary thyroid carcinoma: Report of a large family with expression of the disease only in the homozygous gene carriers
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Author keywords
[No Author keywords available]
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Indexed keywords
PENTAGASTRIN;
PROTEIN RET;
ADOLESCENT;
ADULT;
ARTICLE;
BIOCHEMISTRY;
CELL HYPERPLASIA;
CHILD;
CONSANGUINEOUS MARRIAGE;
DISEASE COURSE;
FAMILIAL CANCER;
FAMILY;
FEMALE;
GENE MUTATION;
GENETIC ANALYSIS;
HISTOLOGY;
HOMOZYGOSITY;
HUMAN;
HUMAN TISSUE;
HYPERPARATHYROIDISM;
MAJOR CLINICAL STUDY;
MALE;
PHEOCHROMOCYTOMA;
PRIORITY JOURNAL;
PROTO ONCOGENE;
PROVOCATION TEST;
THYROID MEDULLARY CARCINOMA;
THYROIDECTOMY;
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EID: 0036255690
PISSN: 00396060
EISSN: None
Source Type: Journal
DOI: 10.1067/msy.2002.123006 Document Type: Article |
Times cited : (41)
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References (27)
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