Hereditary cancer predisposition in children: genetic basis and clinical implications (Q36461758)

14 August 2017

1 reference

title

Hereditary cancer predisposition in children: genetic basis and clinical implications (English)

1 reference

14 August 2017

Brigitte Strahm

1 reference

14 August 2017

David Malkin

series ordinal

1 reference

14 August 2017

language of work or name

English

0 references

publication date

1 November 2006

1 reference

International Journal of Cancer

14 August 2017

published in

1 reference

14 August 2017

volume

119

1 reference

14 August 2017

1 reference

14 August 2017

page(s)

2001-2006

1 reference

Hereditary cancer predisposition syndromes

14 August 2017

cites work

1 reference

Cancer genes and the pathways they control

21 January 2018

1 reference

Childhood cancer in the United States. A geographical analysis of cases from the Pediatric Cooperative Clinical Trials groups

21 January 2018

1 reference

Retinoblastoma: revisiting the model prototype of inherited cancer

21 January 2018

1 reference

Mutation and cancer: statistical study of retinoblastoma

21 January 2018

1 reference

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

21 January 2018

1 reference

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

21 January 2018

1 reference

Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells

21 January 2018

1 reference

A long twentieth century of the cell cycle and beyond

21 January 2018

1 reference

The retinoblastoma protein and cell cycle control

21 January 2018

1 reference

Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma

21 January 2018

1 reference

RB1 genetic testing as a clinical service: a follow-up study

21 January 2018

1 reference

Mutations in the p53 gene occur in diverse human tumour types

21 January 2018

1 reference

Sensitivity and predictive value of criteria for p53 germline mutation screening

21 January 2018

1 reference

Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome

21 January 2018

1 reference

The role of p53 in human cancer

21 January 2018

1 reference

ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family data

21 January 2018

1 reference

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

21 January 2018

1 reference

Multiple endocrine neoplasia type 1 (MEN1).

21 January 2018

1 reference

Positional cloning of the gene for multiple endocrine neoplasia-type 1

21 January 2018

1 reference

Characterization of mutations in patients with multiple endocrine neoplasia type 1.

21 January 2018

1 reference

Medullary thyroid carcinoma in children with multiple endocrine neoplasia types 2A and 2B.

21 January 2018

1 reference

Cancer in Fanconi anemia.

21 January 2018

1 reference

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

21 January 2018

1 reference

The Fanconi road to cancer

21 January 2018

1 reference

A Growing Network of Cancer-Susceptibility Genes

21 January 2018

1 reference

21 January 2018

1 reference

Cancer in Fanconi anemia, 1927-2001

21 January 2018

1 reference

Ethical implications of a new application of preimplantation diagnosis.

21 January 2018

1 reference

Preimplantation diagnosis for Fanconi anemia combined with HLA matching

21 January 2018

1 reference

Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/IJC.21962

1 reference

14 August 2017

1 reference