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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2014
Prostate cancer incidence in males with Lynch syndrome
Sigurdis Haraldsdottir, Heather Hampel, Lai Wei, et al.
Genes & Diseases
|
September 11, 2023
Lack of evidence for germline <i>WWP1</i> pathogenic variants in gastrointestinal polyposis and other phenotypes suggestive of PTEN-hamartoma-tumor syndrome
Noemi Gonzalez-Abuin, Tirso Pons, Teresa Fuster, et al.
International Journal of Cancer
|
May 15, 2015
Allele-specific imbalance mapping at human orthologs of mouse susceptibility to colon cancer (Scc) loci
Madelyn M Gerber, Heather Hampel, Xiao-Ping Zhou, et al.
Cancer Research
|
July 17, 2004
Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation
Hidewaki Nakagawa, Janet C Lockman, Wendy L Frankel, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
July 11, 2023
Constitutional MLH1 Methylation Is a Major Contributor to Mismatch Repair-Deficient, MLH1-Methylated Colorectal Cancer in Patients Aged 55 Years and Younger
Megan P Hitchins, Estela Dámaso, Rocio Alvarez, et al.
Plos One
|
May 26, 2012
Evaluation of allele-specific somatic changes of genome-wide association study susceptibility alleles in human colorectal cancers
Madelyn M Gerber, Heather Hampel, Nathan P Schulz, et al.
Stem Cell Reports
|
December 10, 2013
Analysis of induced pluripotent stem cells from a BRCA1 mutant family
Abigail A Soyombo, Yipin Wu, Lauren Kolski, et al.
Human Pathology
|
April 8, 2023
Mismatch repair protein status of non-neoplastic uterine and intestinal mucosa in patients with Lynch syndrome and double somatic mismatch repair protein mutations
C Eric Freitag, Wei Chen, Rachel Pearlman, et al.
Journal of Law and the Biosciences
|
July 5, 2021
What guidance does HIPAA offer to providers considering familial risk notification and cascade genetic testing?
Nora B Henrikson, Jennifer K Wagner, Heather Hampel, et al.
Journal of Genetic Counseling
|
January 28, 2017
Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance
Ilana Solomon, Elizabeth Harrington, Gillian Hooker, et al.
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of 22
Search research articles
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Showing results (81-90 of 215) with videos related to
Sort By:
Page
of 22
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2014
Prostate cancer incidence in males with Lynch syndrome
Sigurdis Haraldsdottir, Heather Hampel, Lai Wei, et al.
Genes & Diseases
|
September 11, 2023
Lack of evidence for germline <i>WWP1</i> pathogenic variants in gastrointestinal polyposis and other phenotypes suggestive of PTEN-hamartoma-tumor syndrome
Noemi Gonzalez-Abuin, Tirso Pons, Teresa Fuster, et al.
International Journal of Cancer
|
May 15, 2015
Allele-specific imbalance mapping at human orthologs of mouse susceptibility to colon cancer (Scc) loci
Madelyn M Gerber, Heather Hampel, Xiao-Ping Zhou, et al.
Cancer Research
|
July 17, 2004
Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation
Hidewaki Nakagawa, Janet C Lockman, Wendy L Frankel, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
July 11, 2023
Constitutional MLH1 Methylation Is a Major Contributor to Mismatch Repair-Deficient, MLH1-Methylated Colorectal Cancer in Patients Aged 55 Years and Younger
Megan P Hitchins, Estela Dámaso, Rocio Alvarez, et al.
Plos One
|
May 26, 2012
Evaluation of allele-specific somatic changes of genome-wide association study susceptibility alleles in human colorectal cancers
Madelyn M Gerber, Heather Hampel, Nathan P Schulz, et al.
Stem Cell Reports
|
December 10, 2013
Analysis of induced pluripotent stem cells from a BRCA1 mutant family
Abigail A Soyombo, Yipin Wu, Lauren Kolski, et al.
Human Pathology
|
April 8, 2023
Mismatch repair protein status of non-neoplastic uterine and intestinal mucosa in patients with Lynch syndrome and double somatic mismatch repair protein mutations
C Eric Freitag, Wei Chen, Rachel Pearlman, et al.
Journal of Law and the Biosciences
|
July 5, 2021
What guidance does HIPAA offer to providers considering familial risk notification and cascade genetic testing?
Nora B Henrikson, Jennifer K Wagner, Heather Hampel, et al.
Journal of Genetic Counseling
|
January 28, 2017
Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance
Ilana Solomon, Elizabeth Harrington, Gillian Hooker, et al.
Page
of 22