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))

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	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
Μορφή:	Journal article
Γλώσσα:	English
Έκδοση:	1996

Παρόμοια τεκμήρια

Clinical studies of multiple endocrine neoplasia type 1 (MEN1) (vol 89, pg 653, 1996)
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Έκδοση: (1996)

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)
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A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1.
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Έκδοση: (2007)

Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 families.
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Έκδοση: (1993)

The molecular basis of parathyroid tumours in multiple endocrine neoplasia type 1
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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.
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Multiple endocrine neoplasia type 1
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Έκδοση: (2012-01-01)

CHROMOSOME-11 ABNORMALITIES IN PARATHYROID TUMORS OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-I (MENTI)
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Multiple endocrine neoplasia type 1.
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Multiple endocrine neoplasia type 1 (MEN1).
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Multiple endocrine neoplasia type 1 (MEN1).
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Multiple endocrine neoplasia
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Multiple endocrine neoplasia.
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Multiple endocrine neoplasia.
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MOLECULAR-GENETIC MAPPING OF 13 MARKERS FROM CHROMOSOME-11Q13 IN 33 FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-1
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The role of molecular genetics in screening for multiple endocrine neoplasia type 1.
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Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene.
ανά: Pang, J, κ.ά.
Έκδοση: (1996)

MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 - GENETIC AND BIOCHEMICAL SCREENING OF A FAMILY
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Molecular genetic mapping of the multiple endocrine neoplasia type 1 locus.
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Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36.
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Role of multiple endocrine neoplasia type 1 mutational analysis in clinical practice.
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The molecular genetics of the multiple endocrine neoplasia syndromes.
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Multiple endocrine neoplasia--syndromes of the twentieth century.
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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).
ανά: Lloyd, SE, κ.ά.
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Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).
ανά: Thakker, R, κ.ά.
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Proliferation rates of multiple endocrine neoplasia type 1 (MEN1)-associated tumors.
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Multiple endocrine neoplasia type 1
ανά: Luzi Ettore, κ.ά.
Έκδοση: (2006-10-01)

Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1.
ανά: Bassett, J, κ.ά.
Έκδοση: (1999)

Meta-analysis of 31 studies reporting 344 mutations in the multiple endocrine neoplasia type 1 (MEN1) gene.
ανά: Pannett, A, κ.ά.
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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.
ανά: Lemos, M, κ.ά.
Έκδοση: (2008)

Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1.
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Έκδοση: (2002)

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene
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Έκδοση: (1997)

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.
ανά: Pannett, A, κ.ά.
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The European Consortium on MEN1 - Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)
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Έκδοση: (1997)