MEN1 gene alterations do not correlate with the phenotype of sporadic primary hyperparathyroidism

Journal of Endocrinological Investigation

Volumn 25, Issue 6, 2002, Pages 508-512

  Cetani, F ^a   Pardi, E ^a   Vignali, E ^a   Borsari, S ^a   Picone, A ^a   Cianferotti, L ^a   Ambrogini, E ^a   Miccoli, P ^a   Pinchera, A ^a   Marcocci, C ^a  

^a UNIVERSITY OF PISA   (Italy)

Author keywords

LOH; MEN1 gene; Menin; Primary hyperparathyroidism

Indexed keywords

MICROSATELLITE DNA;

ADENOMA; ARTICLE; CHROMOSOME 11; DNA SEQUENCE; FEMALE; GENETICS; HETEROZYGOSITY LOSS; HUMAN; HYPERPARATHYROIDISM; MALE; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA; MUTATION; NUCLEOTIDE SEQUENCE; PARATHYROID TUMOR; PHENOTYPE; ADULT; AGED; BIOCHEMISTRY; CHROMOSOME 11Q; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; EXON; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; GENETIC DISORDER; GENETIC HETEROGENEITY; GENOTYPE PHENOTYPE CORRELATION; MICROSATELLITE MARKER; PRIMARY HYPERPARATHYROIDISM;

ADENOMA; CHROMOSOMES, HUMAN, PAIR 11; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; HYPERPARATHYROIDISM; LOSS OF HETEROZYGOSITY; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; MUTATION; PARATHYROID NEOPLASMS; PHENOTYPE; SEQUENCE ANALYSIS, DNA;

EID: 0035987929     PISSN: 03914097     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF03345492     Document Type: Article

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