Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Molly Deacon"'
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Supplementary Table 1 from Origins and Prevalence of the American Founder Mutation of MSH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03a312ce5bd2554b5b8aa100e29f6b73
https://doi.org/10.1158/0008-5472.22370685.v1
https://doi.org/10.1158/0008-5472.22370685.v1
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Supplementary Figure 1 from Origins and Prevalence of the American Founder Mutation of MSH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e21b3ce9f79af67b38f086b2d56f94f
https://doi.org/10.1158/0008-5472.22370688.v1
https://doi.org/10.1158/0008-5472.22370688.v1
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Supplementary Table 2 from Origins and Prevalence of the American Founder Mutation of MSH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f35983558639f12401ff99760e775b25
https://doi.org/10.1158/0008-5472.22370682.v1
https://doi.org/10.1158/0008-5472.22370682.v1
Autor:
Albert de la Chapelle, Heather Hampel, Henry T. Lynch, Stephen N. Thibodeau, Brittany C. Thomas, Gordon Gong, Jane F. Lynch, Molly Deacon, Ilene Comeras, Victoria Schunemann, Dan Fix, Sandya Liyanarachchi, Kyle Walsh, Shuying Sun, Mark E. Baze, Mark Clendenning
Large germline deletions within the mismatch repair gene MSH2 account for a significant proportion (up to 20%) of all deleterious mutations of this gene which are associated with Lynch syndrome. An exons 1 to 6 deletion of MSH2, originally reported i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c191f3329d9a72241f6091604193cc13
https://doi.org/10.1158/0008-5472.c.6496491.v1
https://doi.org/10.1158/0008-5472.c.6496491.v1
Autor:
Mark Clendenning, Heather Hampel, Shuying Sun, Brittany C. Thomas, Molly Deacon, Victoria Schunemann, Sandya Liyanarachchi, Gordon Gong, Henry T. Lynch, Dan Fix, Albert de la Chapelle, Jane F. Lynch, Kyle M. Walsh, Ilene Comeras, Stephen N. Thibodeau, Mark E. Baze
Publikováno v:
Cancer Research. 68:2145-2153
Large germline deletions within the mismatch repair gene MSH2 account for a significant proportion (up to 20%) of all deleterious mutations of this gene which are associated with Lynch syndrome. An exons 1 to 6 deletion of MSH2, originally reported i