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Acta Gastroenterologica Latinoamericana
|
October 25, 2007
[Hereditary diffuse gastric cancer (HDGC): presentation of a family with a new mutation of the CDH1 gene]
Fernando Van Domselaar, Daniel Correa, Carlos Vaccaro, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 15, 2018
Common genetic variants contribute to incomplete penetrance: evidence from cancer-free BRCA1 mutation carriers
Bradley Downs, Simon Sherman, Jian Cui, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 14, 2008
Mutational load distribution analysis yields metrics reflecting genetic instability during pancreatic carcinogenesis
Gemma Tarafa, David Tuck, Daniela Ladner, et al.
Disease Markers
|
July 20, 2004
SELDI-TOF serum profiling for prognostic and diagnostic classification of breast cancers
Christine Laronga, Stephen Becker, Patrice Watson, et al.
The Breast Journal
|
June 27, 2013
Can unknown predisposition in familial breast cancer be family-specific?
Henry Lynch, Hongxiu Wen, Yeong C Kim, et al.
The American Journal of Gastroenterology
|
April 20, 2004
Multicenter experience with upper gastrointestinal polyps in pediatric patients with familial adenomatous polyposis
Thomas M Attard, Carmen Cuffari, Tanya Tajouri, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 13, 2019
Variants of DNA mismatch repair genes derived from 33,998 Chinese individuals with and without cancer reveal their highly ethnic-specific nature
Li Zhang, Shanmuga Priya Bhaskaran, Teng Huang, et al.
BMC Cancer
|
June 3, 2014
Genome instability in blood cells of a BRCA1+ breast cancer family
Fengxia Xiao, Yeong C Kim, Carrie Snyder, et al.
Blood
|
May 19, 2011
Paraproteins of familial MGUS/multiple myeloma target family-typical antigens: hyperphosphorylation of autoantigens is a consistent finding in familial and sporadic MGUS/MM
Sandra Grass, Klaus-Dieter Preuss, Stephan Thome, et al.
Genes, Chromosomes & Cancer
|
August 31, 2002
A 10-Mb paracentric inversion of chromosome arm 2p inactivates MSH2 and is responsible for hereditary nonpolyposis colorectal cancer in a North-American kindred
Anja Wagner, Heleen van der Klift, Patrick Franken, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 52) with videos related to
Sort By:
Page
of 6
Acta Gastroenterologica Latinoamericana
|
October 25, 2007
[Hereditary diffuse gastric cancer (HDGC): presentation of a family with a new mutation of the CDH1 gene]
Fernando Van Domselaar, Daniel Correa, Carlos Vaccaro, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 15, 2018
Common genetic variants contribute to incomplete penetrance: evidence from cancer-free BRCA1 mutation carriers
Bradley Downs, Simon Sherman, Jian Cui, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 14, 2008
Mutational load distribution analysis yields metrics reflecting genetic instability during pancreatic carcinogenesis
Gemma Tarafa, David Tuck, Daniela Ladner, et al.
Disease Markers
|
July 20, 2004
SELDI-TOF serum profiling for prognostic and diagnostic classification of breast cancers
Christine Laronga, Stephen Becker, Patrice Watson, et al.
The Breast Journal
|
June 27, 2013
Can unknown predisposition in familial breast cancer be family-specific?
Henry Lynch, Hongxiu Wen, Yeong C Kim, et al.
The American Journal of Gastroenterology
|
April 20, 2004
Multicenter experience with upper gastrointestinal polyps in pediatric patients with familial adenomatous polyposis
Thomas M Attard, Carmen Cuffari, Tanya Tajouri, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 13, 2019
Variants of DNA mismatch repair genes derived from 33,998 Chinese individuals with and without cancer reveal their highly ethnic-specific nature
Li Zhang, Shanmuga Priya Bhaskaran, Teng Huang, et al.
BMC Cancer
|
June 3, 2014
Genome instability in blood cells of a BRCA1+ breast cancer family
Fengxia Xiao, Yeong C Kim, Carrie Snyder, et al.
Blood
|
May 19, 2011
Paraproteins of familial MGUS/multiple myeloma target family-typical antigens: hyperphosphorylation of autoantigens is a consistent finding in familial and sporadic MGUS/MM
Sandra Grass, Klaus-Dieter Preuss, Stephan Thome, et al.
Genes, Chromosomes & Cancer
|
August 31, 2002
A 10-Mb paracentric inversion of chromosome arm 2p inactivates MSH2 and is responsible for hereditary nonpolyposis colorectal cancer in a North-American kindred
Anja Wagner, Heleen van der Klift, Patrick Franken, et al.
Page
of 6