scholarly article | Q13442814 |
P356 | DOI | 10.1002/(SICI)1097-0215(19971210)73:6<831::AID-IJC11>3.0.CO;2-7 |
P698 | PubMed publication ID | 9399661 |
P50 | author | Alain Puisieux | Q56422488 |
P2093 | author name string | Q Wang | |
M Ozturk | |||
C Navarro | |||
F Desseigne | |||
G Luleci | |||
I Keser | |||
J A Chayvialle | |||
C Lasset | |||
J C Saurin | |||
T Gelen | |||
H Bagci | |||
T Yagci | |||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Lynch syndrome | Q783644 |
P304 | page(s) | 831-836 | |
P577 | publication date | 1997-12-01 | |
P1433 | published in | International Journal of Cancer | Q332492 |
P1476 | title | Germline hMSH2 and hMLH1 gene mutations in incomplete HNPCC families | |
P478 | volume | 73 |
Q45805261 | Analysis of mismatch repair gene mutations in Turkish HNPCC patients. |
Q58006247 | Clinical Definition of Hereditary Non-polyposis Colorectal Cancer: A Search for the Impossible? |
Q38024724 | Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome. |
Q36641429 | Extensive molecular screening for hereditary non-polyposis colorectal cancer |
Q35355789 | Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis |
Q53302615 | High risk for neoplastic transformation of endometriosis in a carrier of Lynch syndrome. |
Q50919937 | Ikaros is a mutational target for lymphomagenesis in Mlh1-deficient mice. |
Q38301022 | Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation. |
Q53421519 | Predominant germ-line mutation of the hMSH2 gene in Japanese hereditary non-polyposis colorectal cancer kindreds. |
Q34633911 | Prevalence of pathological germline mutations of hMLH1 and hMSH2 genes in colorectal cancer |
Q51956436 | Systematic mRNA analysis for the effect of MLH1 and MSH2 missense and silent mutations on aberrant splicing. |