Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism

Clinical Endocrinology

Volumn 58, Issue 5, 2003, Pages 639-646

  Pannett, A A J ^a,b   Kennedy, A M ^b   Turner, J J O ^b   Forbes, S A ^a   Cavaco, B M ^a,b   Bassett, J H D ^a   Cianferotti, L ^a   Harding, B ^a,b   Shine, B ^c   Flinter, F ^d   Maidment, C G H ^e   Trembath, R ^f   Thakker, R V ^a,b  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^d GUY S HOSPITAL   (United Kingdom)

^e WEXHAM PARK HOSPITAL   (United Kingdom)

^f LEICESTER ROYAL INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ALLELE; ARTICLE; CANCER INHIBITION; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; FAMILIAL CANCER; FEMALE; FOLLOW UP; GENE LOSS; GENE MUTATION; HETEROZYGOSITY; HUMAN; HYPERPARATHYROIDISM; MALE; MISSENSE MUTATION; MULTIPLE ENDOCRINE NEOPLASIA; PARATHYROID TUMOR; PRIORITY JOURNAL; SEQUENCE ANALYSIS; WILD TYPE;

ADENOMA; ADOLESCENT; ADULT; AGED; FAMILY HEALTH; FEMALE; GENE DELETION; GERM-LINE MUTATION; HUMANS; HYPERPARATHYROIDISM; HYPERPLASIA; MALE; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; MUTATION, MISSENSE; PARATHYROID GLANDS; PARATHYROID HORMONE; PARATHYROID NEOPLASMS; PEDIGREE; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA;

EID: 0038332150     PISSN: 03000664     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2265.2003.01765.x     Document Type: Article

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