相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Yield of routine molecular analyses in colorectal cancer patients=70 years to detect underlying Lynch syndrome
Margot G. F. van Lier et al.
JOURNAL OF PATHOLOGY (2012)
Pitfalls in molecular analysis for mismatch repair deficiency in a family with biallelic pms2 germline mutations
C. H. M. Leenen et al.
CLINICAL GENETICS (2011)
Pathology, genetics and cytogenetics of Wilms' tumour
Reena Md Zin et al.
PATHOLOGY (2011)
Subtype-Specific FBXW7 Mutation and MYCN Copy Number Gain in Wilms' Tumor
Richard D. Williams et al.
CLINICAL CANCER RESEARCH (2010)
On the advent of MSI testing of all colorectal cancers and a substantial part of other Lynch syndrome-related neoplasms
Winand N. M. Dinjens et al.
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS (2010)
A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory
Margot G. F. van Lier et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2010)
Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications
H. T. Lynch et al.
CLINICAL GENETICS (2009)
Do Microsatellite Instability Profiles Really Differ Between Colorectal and Endometrial Tumors?
Ana M. Ferreira et al.
GENES CHROMOSOMES & CANCER (2009)
Biallelic germline mutations of mismatch-repair genes - A possible cause for multiple pediatric malignancies
Jan-Werner Poley et al.
CANCER (2007)
Role of the BRAF mutations in the microsatellite instability genetic pathway in sporadic colorectal cancer
M. L. Maestro et al.
ANNALS OF SURGICAL ONCOLOGY (2007)
Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics
Kristina Lagerstedt Robinson et al.
JOURNAL OF THE NATIONAL CANCER INSTITUTE (2007)
Malignant renal tumours incidence and survival in European children (1978-1997): Report from the Automated Childhood Cancer Information System Project
Guido Pastore et al.
EUROPEAN JOURNAL OF CANCER (2006)
Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours
Y. Satoh et al.
BRITISH JOURNAL OF CANCER (2006)
Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour
R. H. Scott et al.
JOURNAL OF MEDICAL GENETICS (2006)
Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations
P Bandipalliam
FAMILIAL CANCER (2005)
Mismatch repair and DNA damage signalling
L Stojic et al.
DNA REPAIR (2004)
BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer
GR Deng et al.
CLINICAL CANCER RESEARCH (2004)
Role of DNA mismatch repair defects in the pathogenesis of human cancer
P Peltomäki
JOURNAL OF CLINICAL ONCOLOGY (2003)
Evaluation of tumor microsatellite instability using five quasi monomorphic mononucleotide repeats and pentaplex PCR
N Suraweera et al.
GASTROENTEROLOGY (2002)
DNA mismatch repair and cancer
P Peltomäki
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH (2001)
16q loss of heterozygosity and microsatellite instability in Wilms' tumor
JE Mason et al.
JOURNAL OF PEDIATRIC SURGERY (2000)