Mutation analysis of the MEN1 gene in Israeli patients with MEN1 and familial isolated hyperprolactinemia.

Human mutation

Volumn 16, Issue 3, 2000, Pages 269-

  Jakobovitz Picard, O ^a   Olchovsky, D ^a   Berezin, M ^a   Ghodsizade, A ^a   Zahavi, Z ^a   Karasik, A ^a   Rechavi, G ^a   Friedman, E ^a  

^a GERTNER INSTITUTE FOR EPIDEMIOLOGY AND HEALTH POLICY RESEARCH   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

MEN1 PROTEIN, HUMAN; ONCOPROTEIN; TUMOR PROTEIN;

ADOLESCENT; ADULT; ARTICLE; FEMALE; GENE DELETION; GENETICS; HAPLOTYPE; HUMAN; ISRAEL; MALE; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; TUMOR SUPPRESSOR GENE;

ADOLESCENT; ADULT; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, TUMOR SUPPRESSOR; GERM-LINE MUTATION; HAPLOTYPES; HUMANS; ISRAEL; MALE; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; NEOPLASM PROTEINS; PEDIGREE; PROTO-ONCOGENE PROTEINS; SEQUENCE DELETION;

MLCS; MLOWN;

EID: 0034267569     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/1098-1004(200009)16:3<269::aid-humu11>3.0.co;2-2     Document Type: Article

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