(Q40850830)

24 September 2017

title

Allele loss in Wilms tumors of chromosome arms 11q, 16q, and 22q correlate with clinicopathological parameters (English)

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24 September 2017

9

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24 September 2017

Klamt B

1

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24 September 2017

Schulze M

2

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24 September 2017

Thäte C

3

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24 September 2017

Mares J

4

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24 September 2017

Goetz P

5

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24 September 2017

Kodet R

6

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24 September 2017

Scheulen W

7

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24 September 2017

Weirich A

8

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24 September 2017

Gessler M

10

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24 September 2017

publication date

1 August 1998

1 reference

Genes, Chromosomes and Cancer

24 September 2017

published in

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24 September 2017

volume

22

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24 September 2017

issue

4

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24 September 2017

page(s)

287-294

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Single nucleotide polymorphisms in the human E-cadherin gene.

24 September 2017

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Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

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Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination

21 January 2018

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Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

21 January 2018

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Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.

21 January 2018

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Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer

21 January 2018

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Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

21 January 2018

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Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome

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A clinical overview of WT1 gene mutations

21 January 2018

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Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors

21 January 2018

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Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

21 January 2018

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Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells

21 January 2018

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Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology

21 January 2018

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Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor

21 January 2018

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Fine structure analysis of the WT1 gene in sporadic Wilms tumors

21 January 2018

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Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis

21 January 2018

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Infrequent mutation of theWT1 gene in 77 Wilms' tumors

21 January 2018

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Mapping of a Putative Tumor Suppressor Locus to Proximal 7p in Wilms Tumors

21 January 2018

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Allelotyping in Wilms Tumors Identifies a Putative Third Tumor Suppressor Gene on Chromosome 11

21 January 2018

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Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutations

21 January 2018

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Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: a preliminary analysis

21 January 2018

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Allelic imbalance at chromosome 1q21 in Wilms tumor

21 January 2018

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Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

21 January 2018

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A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region

21 January 2018

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Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors

21 January 2018

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Comparative genomic hybridization analysis of Wilms tumors

21 January 2018

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10.1002/(SICI)1098-2264(199808)22:4<287::AID-GCC4>3.0.CO;2-R

21 January 2018

Identifiers

DOI

1 reference

24 September 2017

1 reference