Corrigendum: Clinical studies of multiple endocrine neoplasia type 1 (MEN1) (Q J Med (1996) 89 (653-659))

Corrigendum: Clinical studies of multiple endocrine neoplasia type 1 (MEN1) (Q J Med (1996) 89 (653-659))

Bibliografiska uppgifter
Huvudupphovsmän:	Trump, D, Farren, B, Wooding, C, Pang, J, Besser, G, Buchanan, K, Edwards, C, Heath, D, Jackson, C, Jansen, S, Shalet, S, Wheeler, M, Zink, A, Thakker, R
Materialtyp:	Journal article
Språk:	English
Publicerad:	1996

Liknande verk

Clinical studies of multiple endocrine neoplasia type 1 (MEN1) (vol 89, pg 653, 1996)
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Characterization of mutations in patients with multiple endocrine neoplasia type 1.
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Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11.
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Multiple endocrine neoplasia type 1 (MEN1).
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Multiple endocrine neoplasia type 1 (MEN1).
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Molecular genetic mapping of the multiple endocrine neoplasia type 1 locus.
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Prolactinoma presenting in identical twins with multiple endocrine neoplasia type 1.
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Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).
av: Lloyd, SE, et al.
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Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).
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Proliferation rates of multiple endocrine neoplasia type 1 (MEN1)-associated tumors.
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Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1.
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Meta-analysis of 31 studies reporting 344 mutations in the multiple endocrine neoplasia type 1 (MEN1) gene.
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Diagnostic challenges due to phenocopies: lessons from Multiple Endocrine Neoplasia type1 (MEN1).
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Molecular genetics and patient management of multiple endocrine neoplasia type I
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Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene.
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Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1.
av: Turner, J, et al.
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Identification of the multiple endocrine neoplasia type 1 (MEN1) gene
av: Lemmens, I, et al.
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Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.
av: Pannett, A, et al.
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The European Consortium on MEN1 - Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)
av: Bassett, J, et al.
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