Identification of genetic susceptibility to childhood cancer through analysis of genes in parallel (Q42013225)

15 October 2017

Identification of genetic susceptibility to childhood cancer through analysis of genes in parallel (English)

1 reference

15 October 2017

1 reference

9

Donna M Muzny

1 reference

15 October 2017

12

Richard A Gibbs

1 reference

15 October 2017

Sharon E Plon

1

1 reference

15 October 2017

David A Wheeler

2

1 reference

15 October 2017

Louise C Strong

3

1 reference

15 October 2017

Gail E Tomlinson

4

1 reference

15 October 2017

Michael Pirics

5

1 reference

15 October 2017

Qingchang Meng

6

1 reference

15 October 2017

Hannah C Cheung

7

1 reference

15 October 2017

Phyllis R Begin

8

1 reference

15 October 2017

Lora Lewis

10

1 reference

15 October 2017

Jaclyn A Biegel

11

1 reference

15 October 2017

1 January 2011

1 reference

15 October 2017

1 reference

15 October 2017

204

1 reference

15 October 2017

19-25

1 reference

15 October 2017

1

1 reference

Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors

15 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Common variants in human CRC genes as low-risk alleles

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Identification of ALK as a major familial neuroblastoma predisposition gene

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Utility of oligonucleotide array-based comparative genomic hybridization for detection of target gene deletions.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Germline mutation of INI1/SMARCB1 in familial schwannomatosis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

The consensus coding sequences of human breast and colorectal cancers

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Predisposition to atypical teratoid/rhabdoid tumor due to an inherited INI1 mutation

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

SNPdetector: a software tool for sensitive and accurate SNP detection

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Inherited susceptibility for pediatric cancer.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatin

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Polymorphisms and HNPCC: PMS2-MLH1 protein interactions diminished by single nucleotide polymorphisms

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

HRAS mutation analysis in Costello syndrome: genotype and phenotype correlation.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Chromosomal fragility syndrome and family history of radiosensitivity as indicators for radiotherapy dose modification

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Multiple Tumors in a Child with Germ-Line Mutations inTP53andPTEN

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075924

Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21356188

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1000 Genomes Project promises closer look at variation in human genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21356188

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21356188

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.CANCERGENCYTO.2010.11.001

1 reference

15 October 2017

1 reference

15 October 2017

1 reference