Genetic predisposition and screening in pediatric cancer (Q35064135)

6 August 2017

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title

Genetic predisposition and screening in pediatric cancer (English)

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6 August 2017

1

Samart Pakakasama

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6 August 2017

Gail E Tomlinson

2

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6 August 2017

1 December 2002

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Pediatric Clinics of North America

6 August 2017

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6 August 2017

49

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6 August 2017

6

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6 August 2017

1393-1413

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Mutation and cancer: statistical study of retinoblastoma

6 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Patterns of risk of hereditary retinoblastoma and applications to genetic counselling

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Trilateral retinoblastoma: a meta-analysis of hereditary retinoblastoma associated with primary ectopic intracranial retinoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Retinoma: spontaneous regression of retinoblastoma or benign manifestation of the mutation?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Retinoblastoma: the disease, gene and protein provide critical leads to understand cancer.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Germline mutations in the RB1 gene in patients with hereditary retinoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Deletion of RB exons 24 and 25 causes low-penetrance retinoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

A splicing mutation in RB1 in low penetrance retinoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Second primary neoplasms in patients with retinoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Mortality from second tumors among long-term survivors of retinoblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Cancer incidence after retinoblastoma. Radiation dose and sarcoma risk

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Hereditary retinoblastoma, lipoma, and second primary cancers

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Prediction of the Risk of Hereditary Retinoblastoma, Using DNA Polymorphisms within the Retinoblastoma Gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

At what age could screening for familial retinoblastoma be stopped? A register based study 1945-98.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Population-based risk estimates of Wilms tumor in sporadic aniridia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Germline WT1 mutations in Wilms' tumor patients: preliminary results

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Renal hamartomas and nephroblastomatosis with fetal gigantism: a familial syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Nephromegaly in infancy and early childhood: a risk factor for Wilms tumor in Beckwith-Wiedemann syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Characteristics and outcome of children with Beckwith-Wiedemann syndrome and Wilms' tumor: a report from the National Wilms Tumor Study Group

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Familial Wilms' tumor: a descriptive study

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Screening for Wilms tumor and hepatoblastoma in children with Beckwith-Wiedemann syndromes: a cost-effective model

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

High frequency of germline p53 mutations in childhood adrenocortical cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

The genetic testing of children for cancer susceptibility: ethical, legal, and social issues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Recommendations on predictive testing for germ line p53 mutations among cancer-prone individuals

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Mutations of the hSNF5/INI1 Gene in Renal Rhabdoid Tumors With Second Primary Brain Tumors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Von Hippel-Lindau Syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

von Hippel-Lindau disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

A genetic register for von Hippel-Lindau disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Identification of the von Hippel-Lindau disease tumor suppressor gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Functions of the von Hippel-Lindau tumour suppressor protein

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

The von Hippel-Lindau tumor suppressor gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Germline mutation profile of theVHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Mosaicism in von Hippel-Lindau disease: lessons from kindreds with germline mutations identified in offspring with mosaic parents

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Cancer in ataxia-telangiectasia patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

A single ataxia telangiectasia gene with a product similar to PI-3 kinase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Ataxia-telangiectasia, cancer and the pathobiology of the ATM gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Malignancies in pediatric patients with ataxia telangiectasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Incidence of cancer in 161 families affected by ataxia-telangiectasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Bloom's syndrome. XX. The first 100 cancers

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Bloom's syndrome. III. Analysis of the chromosome aberration characteristic of this disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Chromosomal aberrations in Bloom syndrome patients with myeloid malignancies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

The Bloom's syndrome gene product is homologous to RecQ helicases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Positional cloning of the Werner's syndrome gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Werner's syndrome: what does an aging syndrome gene reveal about cancer?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Mucosal ganglioneuromatosis, medullary thyroid carcinoma, and pheochromocytoma: multiple endocrine neoplasia, type 2b

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

The syndrome of multiple aucosal neuromas and medullary thyroid carcinoma in childhood. Importance of recognition of the phenotype for the early detection of malignancy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Natural history of familial medullary thyroid carcinoma: effect of a program for early diagnosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Medullary carcinoma in children. Results of early detection and surgery

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Predictive DNA testing for multiple endocrine neoplasia 2: a therapeutic challenge of prophylactic thyroidectomy in very young children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Extracolonic manifestations of familial polyposis coli

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Desmoid tumours in familial adenomatous polyposis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Diagnostic value of fundus examination in familial adenomatous polyposis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Increased risk of thyroid and pancreatic carcinoma in familial adenomatous polyposis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Malignant tumors of the central nervous system associated with familial polyposis of the colon: report of two cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

The molecular basis of Turcot's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Gardner syndrome in a man with an interstitial deletion of 5q.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Localization of the gene for familial adenomatous polyposis on chromosome 5.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

The gene for familial polyposis coli maps to the long arm of chromosome 5.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Variable phenotype of familial adenomatous polyposis in pedigrees with 3' mutation in the APC gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Screening for familial adenomatous polyposis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

The effect of celecoxib, a cyclooxygenase-2 inhibitor, in familial adenomatous polyposis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of molecularly defined subtypes of childhood acute leukemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Defending genome integrity during DNA replication: a proposed role for RecQ family helicases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Risk of hepatoblastoma in familial adenomatous polyposis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Hepatocellular carcinoma in children associated with Gardner syndrome or familial adenomatous polyposis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Breast and other cancers in families with ataxia-telangiectasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2802%2900095-0

10.1016/S0031-3955(02)00095-0

7 January 2021

Identifiers

DOI

1 reference

6 August 2017

1 reference

PubMed ID

12580371