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Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome

Michael P. Farrell; David J. Hughes; Ian R. Berry; David J. Gallagher; Emily A. Glogowski; Stewart J. Payne; Michael J. Kennedy; Róisín M. Clarke; Susan A. White; Cian B. Muldoon; Fiona Macdonald; Pauline Rehal; Danielle Crompton; Solvig Roring; Sarah T. Duke; Trudi McDevitt; David E. Barton; Shirley V. Hodgson; Andrew J. Green; Peter A. Daly
Familial Cancer · Vol. 11, Issue 3 · pp. 509-518 · 2012

Abstract

Abstract is unavailable.

Bibliographic Information

JournalFamilial Cancer
PublisherSpringer
Publication Date2012-09-01
Publication Year2012
Volume11
Issue3
Pages509-518
Document TypeJournal Article
eISSN1573-7292
DOI10.1007/s10689-012-9544-4

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NARA Access Coverage2001-01-01~Current
Journal Homepagehttps://www.springer.com/journal/10689
Publisher PageOpen Publisher Page
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