Familial Infiltrative Fibromatosis (Desmoid Tumours) (MIM135290) Caused by a Recurrent 3′ APC Gene Mutation

Author： Scott Rodney J.   Froggatt Nicola J.   Trembath Richard C.   Evans D. Gareth R.   Hodgson Shirley V.   Maher Eamonn R.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.5, Iss.12, 1996-12, pp. : 1921-1924

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Hereditary Desmoid Disease in a Family with a Germline Alu I Repeat Mutation of the APC Gene

By  

Human Heredity, Vol. 49, Iss. 2, 1999-03 ,pp. : 97-102

Karger

Access to resources Recommend Favorite

APC mutations in FAP-associated desmoid tumours are non-random but not ‘just right’

By Latchford Andrew   Volikos Emmanouil   Johnson Victoria   Rogers Pauline   Suraweera Nirosha   Tomlinson Ian   Phillips Robin   Silver Andrew  

Human Molecular Genetics, Vol. 16, Iss. 1, 2007-01 ,pp. : 78-82

Oxford University Press

Access to resources Recommend Favorite

Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

By Eldadah Z.A.  

Human Molecular Genetics, Vol. 10, Iss. 2, 2001-01 ,pp. : 163-169

Oxford University Press

Access to resources Recommend Favorite

-Catenin degradation mediated by the CID domain of APC provides a model for the selection of APC mutations in colorectal, desmoid and duodenal tumours

By Kohler Eva Maria   Chandra Shree Harsha Vijaya   Behrens Jrgen   Schneikert Jean  

Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. : 213-226

Oxford University Press

Access to resources Recommend Favorite

Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin , a large novel gene

By Davy Brian E.   Robinson Michael L.  

Human Molecular Genetics, Vol. 12, Iss. 10, 2003-05 ,pp. : 1163-1170

Oxford University Press

Access to resources Recommend Favorite