rdf:type |
|
lifeskim:mentions |
umls-concept:C0007097,
umls-concept:C0015565,
umls-concept:C0015576,
umls-concept:C0039082,
umls-concept:C0205182,
umls-concept:C0206530,
umls-concept:C0231449,
umls-concept:C0241888,
umls-concept:C0324740,
umls-concept:C0525037,
umls-concept:C1836717
|
pubmed:issue |
1
|
pubmed:dateCreated |
2002-1-29
|
pubmed:abstractText |
Hereditary pancreatic carcinoma shows extant phenotypic and genotypic heterogeneity as evidenced by its integral association with a variety of hereditary cancer syndromes inclusive of the familial atypical multiple mole melanoma (FAMMM) syndrome in concert with CDKN2A (p16) germline mutations.
|
pubmed:grant |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0008-543X
|
pubmed:author |
pubmed-author:BrandRandall ERE,
pubmed-author:DetersCarolyn ACA,
pubmed-author:FusaroRamon MRM,
pubmed-author:GogginsMichaelM,
pubmed-author:HoggDavidD,
pubmed-author:KernScottS,
pubmed-author:KnezeticJosephJ,
pubmed-author:LabiF LFL,
pubmed-author:LassamNorman JNJ,
pubmed-author:LynchHenry THT,
pubmed-author:LynchJane FJF
|
pubmed:copyrightInfo |
Copyright 2002 American Cancer Society.
|
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
94
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
84-96
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:11815963-Adult,
pubmed-meshheading:11815963-Age of Onset,
pubmed-meshheading:11815963-Aged,
pubmed-meshheading:11815963-Dysplastic Nevus Syndrome,
pubmed-meshheading:11815963-Female,
pubmed-meshheading:11815963-Genes, p16,
pubmed-meshheading:11815963-Germ-Line Mutation,
pubmed-meshheading:11815963-Humans,
pubmed-meshheading:11815963-Male,
pubmed-meshheading:11815963-Melanoma,
pubmed-meshheading:11815963-Middle Aged,
pubmed-meshheading:11815963-Neoplastic Syndromes, Hereditary,
pubmed-meshheading:11815963-Pancreatic Neoplasms,
pubmed-meshheading:11815963-Pedigree,
pubmed-meshheading:11815963-Phenotype,
pubmed-meshheading:11815963-Polymerase Chain Reaction,
pubmed-meshheading:11815963-Skin Neoplasms
|
pubmed:year |
2002
|
pubmed:articleTitle |
Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome.
|
pubmed:affiliation |
Department of Preventive Medicine, Creighton University School of Medicine, Omaha, Nebraska 68178, USA. trlynch@creighton.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|