Normal view MARC view ISBD view

Preoperative chemoradiotherapy for esophageal or junctional cancer. [electronic resource]

By:

van Hagen, P

Contributor(s): Producer: 20120605Description: 2074-84 p. digitalISSN:

1533-4406

Subject(s):

Online resources:

Available from publisher's website

In: The New England journal of medicine vol. 366

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, Non-U.S. Gov't

There are no comments on this title.

to post a comment.

Back to results

1 SSCP (single strand conformation polymorphism) analysis of PCR fragments.
by Yandell, D W
2 How sensitive is PCR-SSCP?
by Hayashi, K
3 Genetics of retinoblastoma: implications for other human cancers.
by Yandell, D W
4 p53 analysis in diagnostic pathology. Biologic implications and possible clinical applications.
by Yandell, D W
5 Detection of DNA sequence polymorphisms by enzymatic amplification and direct genomic sequencing.
by Yandell, D W
6 Chromosome 14 marker appearance in a human B lymphoblastoid cell line of nonmalignant origin.
by Yandell, D W
7 Prognostic significance of p53 overexpression in node-negative breast carcinoma: preliminary studies support cautious optimism.
by Thor, A D
8 [Mutations of several tumor suppressor genes in primary retinoblastoma].
by Huang, Q
9 [Gene diagnosis and genetic counselling of Rb gene mutations in retinoblastoma patients and their family members].
by Huang, Q
10 [Distinct Rb gene point mutations in families showing low penetrance of hereditary retinoblastoma].
by Huang, Q
11 Structure and partial genomic sequence of the human retinoblastoma susceptibility gene.
by McGee, T L
12 Evidence for coincident mutations in human lymphoblast clones selected for functional loss of a thymidine kinase gene.
by Li, C Y
13 Molecular genetic analysis of recessive mutations at a heterozygous autosomal locus in human cells.
by Yandell, D W
14 Somatic mutations at a heterozygous autosomal locus in human cells occur more frequently by allele loss than by intragenic structural alterations.
by Yandell, D W
15 Elevated frequency of microsatellite mutations in TK6 human lymphoblast clones selected for mutations at the thymidine kinase locus.
by Li, C Y
16 Deletions and point mutations of p16,p15 gene in primary tumors and tumor cell lines.
by Yonghao, T
17 A comparison of mutation induction at the tk and hprt loci in human lymphoblastoid cells; quantitative differences are due to an additional class of mutations at the autosomal tk locus.
by Liber, H L
18 Molecular mechanisms of spontaneous and induced loss of heterozygosity in human cells in vitro.
by Li, C Y
19 Frequent p53 gene mutations in blast crisis of chronic myelogenous leukemia, especially in myeloid crisis harboring loss of a chromosome 17p.
by Nakai, H
20 A system for assaying homologous recombination at the endogenous human thymidine kinase gene.
by Benjamin, M B