The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population (Q34161196)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population |
scientific article |
Statements
1 reference
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population (English)
1 reference
J N Weitzel
1 reference
W D Foulkes
1 reference
G Rennert
1 reference
K Offit
1 reference
B Bressac-De Paillerets
1 reference
A De La Chapelle
1 reference
I Thiffault
1 reference
S B Gruber
1 reference
N Hamel
1 reference
C Lee
1 reference
A Markowitz
1 reference
A Figer
1 reference
E Friedman
1 reference
D Farber
1 reference
C M T Greenwood
1 reference
J D Bonner
1 reference
K Nafa
1 reference
V Marcus
1 reference
L Tomsho
1 reference
J Gebert
1 reference
F A Macrae
1 reference
C L Gaff
1 reference
P K Gregersen
1 reference
P H Gordon
1 reference
E MacNamara
1 reference
M-C King
1 reference
H Hampel
1 reference
J Boyd
1 reference
G Chong
1 reference
N A Ellis
1 reference
26 November 2002
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference