A s of 1999, it is possible to test selected subjects for carriage of germline mutations in genes responsible for familial adenomatous polyposis (FAP), 1,2 hereditary nonpolyposis colorectal cancer (HNPCC), 3,4 Peutz-Jeghers syndrome, 5 and juvenile polyposis. 6,7 These diseases are heterogeneous ph
β¦ LIBER β¦
Abnormalities of lectin histochemistry in familial polyposis coli and hereditary nonpolyposis colorectal cancer
β Scribed by Jeffrey S. Sams; Henry T. Lynch; Randall W. Burt; Stephen J. Lanspa; C. Richard Boland
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 827 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Clinical challenges in management of fam
β
Patrick M. Lynch
π
Article
π
1999
π
John Wiley and Sons
π
English
β 107 KB
π 2 views
Preventive surgery for colon cancer in f
β
Gabriela MΓΆslein; Steffen Pistorius; Hans-Detlev Saeger; Hans K. Schackert
π
Article
π
2003
π
Springer
π
English
β 154 KB
Genetic counseling and interpretation of
β
Nora Wong; Dana Lasko; RogΓ©rio Rabelo; Leonard Pinsky; Philip H. Gordon; William
π
Article
π
2001
π
Springer
π
English
β 865 KB
Practice Parameters for the Treatment of
π
Article
π
2003
π
Springer
π
English
β 229 KB
Consideration of hereditary nonpolyposis
β
Stacey A. South; Heidi Vance; Carolyn Farrell; Richard A. DiCioccio; Cathy Fahey
π
Article
π
2008
π
John Wiley and Sons
π
English
β 267 KB
π 2 views
Mutation of the hMSH2 gene in two famili
β
Hae Mung Jeon; Patrick M. Lynch; Linda Howard; Jaffer Ajani; Bernard Levin; Mars
π
Article
π
1996
π
John Wiley and Sons
π
English
β 554 KB
Communicated by Sauiu L.C. Woo We examined 18 unrelated individuals who have colorectal cancer or cancers associated with the HNPCC syndrome and have a family history of cancer for mutations in exon 13 of the hMSH2 gene. Two of the 18 individuals had the same previously unreported single-base delet