Germline hMSH2 and hMLH1 gene mutations in incomplete HNPCC families

scientific article published on 01 December 1997

Germline hMSH2 and hMLH1 gene mutations in incomplete HNPCC families is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/(SICI)1097-0215(19971210)73:6<831::AID-IJC11>3.0.CO;2-7
P698PubMed publication ID9399661

P50authorAlain PuisieuxQ56422488
P2093author name stringQ 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
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectLynch syndromeQ783644
P304page(s)831-836
P577publication date1997-12-01
P1433published inInternational Journal of CancerQ332492
P1476titleGermline hMSH2 and hMLH1 gene mutations in incomplete HNPCC families
P478volume73

Reverse relations

cites work (P2860)
Q45805261Analysis of mismatch repair gene mutations in Turkish HNPCC patients.
Q58006247Clinical Definition of Hereditary Non-polyposis Colorectal Cancer: A Search for the Impossible?
Q38024724Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome.
Q36641429Extensive molecular screening for hereditary non-polyposis colorectal cancer
Q35355789Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis
Q53302615High risk for neoplastic transformation of endometriosis in a carrier of Lynch syndrome.
Q50919937Ikaros is a mutational target for lymphomagenesis in Mlh1-deficient mice.
Q38301022Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation.
Q53421519Predominant germ-line mutation of the hMSH2 gene in Japanese hereditary non-polyposis colorectal cancer kindreds.
Q34633911Prevalence of pathological germline mutations of hMLH1 and hMSH2 genes in colorectal cancer
Q51956436Systematic mRNA analysis for the effect of MLH1 and MSH2 missense and silent mutations on aberrant splicing.