(Q55067670)

16 June 2018

review article

1 reference

title

The concise handbook of family cancer syndromes. Mayo Familial Cancer Program. (English)

1 reference

16 June 2018

1

Lindor NM

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16 June 2018

author name string

Greene MH

series ordinal

2

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16 June 2018

language of work or name

English

0 references

publication date

1 July 1998

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16 June 2018

Journal of the National Cancer Institute

published in

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16 June 2018

volume

90

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16 June 2018

issue

14

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16 June 2018

page(s)

1039-1071

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16 June 2018

The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations

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The molecular basis of Turcot's syndrome

21 January 2018

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Risk of hepatoblastoma in familial adenomatous polyposis

21 January 2018

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Occurrence of desmoids in patients with familial adenomatous polyposis of the colon.

21 January 2018

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Epidemiology of familial adenomatous polyposis in Finland: impact of family screening on the colorectal cancer rate and survival

21 January 2018

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Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC

21 January 2018

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Mesenteric fibromatosis complicating familial adenomatous polyposis: predisposing factors and results of treatment

21 January 2018

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Screening practice for familial adenomatous polyposis: the potential for regional registers.

21 January 2018

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Brain tumor-polyposis syndrome: two genetic diseases?

21 January 2018

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https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Risk of gastric cancer among Korean familial adenomatous polyposis patients. Report of three cases

21 January 2018

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https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Overview of screening and management of familial adenomatous polyposis

21 January 2018

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https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Colorectal cancer screening: clinical guidelines and rationale

21 January 2018

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https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Cancer risks in A-T heterozygotes

21 January 2018

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https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Heterozygous ATM mutations do not contribute to early onset of breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Positional cloning of the gene for Nijmegen breakage syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Complications of the naevoid basal cell carcinoma syndrome: results of a population based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

A two-hit model for developmental defects in Gorlin syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Nevoid basal cell carcinoma syndrome: review of 118 affected individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Molecular genetics of Bloom's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Autosomal dominant transmission of the NAME syndrome (nevi, atrial myxoma, mucinosis of the skin and endocrine overactivity).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Founding mutations and Alu-mediated recombination in hereditary colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

The dermatopathology of Cowden's syndrome*

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Tylosis associated with carcinoma of the oesophagus and oral leukoplakia in a large Liverpool family--a review of six generations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

The hereditary palmoplantar keratoses: an updated review and classification

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Identification of the genetic locus for keratosis palmaris et plantaris on chromosome 17 near the RARA and keratin type I genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Fanconi's anemia and malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Cloning of cDNAs for Fanconi's anaemia by functional complementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Familial gastric cancer and immunologic abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

E-cadherin germline mutations in familial gastric cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Helicobacter gastritis and intestinal metaplasia in a gastric cancer family

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Etiological heterogeneity in Hodgkin's disease: HLA linked and unlinked determinants of susceptibility independent of histological concordance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Incidence of familial Hodgkin's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Concordance for Hodgkin's disease in identical twins suggesting genetic susceptibility to the young-adult form of the disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Genetics of cutaneous melanoma and nevi

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Acquired precursors of cutaneous malignant melanoma. The familial dysplastic nevus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Molecular genetics of familial cutaneous melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

A familial syndrome with cutaneous malignant melanoma and cerebral astrocytoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

The familial dysplastic nevus syndrome. Natural history and the impact of screening on prognosis. A study of nine families in the Netherlands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

A Familial Syndrome of Pancreatic Cancer and Melanoma with a Mutation in theCDKN2Tumor-Suppressor Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Multiple Endocrine Neoplasia Type 1: A 10-Year Prospective Screening Study in Four Kindreds*

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Experience with multiple endocrine neoplasia type 1 screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Long-term follow-up of von Recklinghausen neurofibromatosis. Survival and malignant neoplasms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Deletion of the entire NF1 gene detected by the FISH: four deletion patients associated with severe manifestations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Lens opacities in neurofibromatosis 2: further significant correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Hereditary multiple exostoses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

A gene for hereditary multiple exostoses maps to chromosome 19p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Mutation Screening of the EXT1 and EXT2 Genes in Patients with Hereditary Multiple Exostoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Natural history study of hereditary multiple exostoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Familial pancreatic adenocarcinoma: association with diabetes and early molecular diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Familial carotid body tumors: case report and epidemiologic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Familial paragangliomas of the head and neck

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Increased risk for cancer in patients with the Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Increased risk of cancer in the Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Peutz-Jeghers syndrome is caused by mutations in a novel serine threoninekinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Cancer and the Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

21 January 2018

Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Mendelian inheritance of familial prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Prostate Cancer Susceptibility Locus on Chromosome 1q: a Confirmatory Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Mutation of the MXI1 gene in prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Characteristics of Prostate Cancer in Families Potentially Linked to the Hereditary Prostate Cancer 1 (HPC1) Locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Family history and the risk of prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Mutations of the VHL tumour suppressor gene in renal carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Papillary renal cell carcinoma: a clinical, radiologic, and pathologic study of 34 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Translocation (X;1) in papillary renal cell carcinoma. A new cytogenetic subtype

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Original Articles: Kidney Cancer: Hereditary Papillary Renal Cell Carcinoma: Clinical Studies in 10 Families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Hereditary retinoblastoma, lipoma, and second primary cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Constitutional RB1-Gene Mutations in Patients with Isolated Unilateral Retinoblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Second primary tumors in patients with retinoblastoma. A review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Familial testicular cancer: a report of the UK family register, estimation of risk and an HLA class 1 sib-pair analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Familial testicular cancer in Norway and southern Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Candidate regions for a testicular cancer susceptibility gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Familial testicular cancer: report of six cases and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

A cross sectional study of renal involvement in tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Novel mutations detected in the TSC2 gene from both sporadic and familial TSC patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Positional cloning of the Werner's syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Retracted: A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Localization of the gene for Cowden disease to chromosome 10q22–23

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Risk of Cancer in Relatives of Prostate Cancer Probands

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Tylosis oesophageal cancer mapped

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNCI%2F90.14.1039

21 January 2018

Identifiers

DOI

10.1093/JNCI/90.14.1039

1 reference

16 June 2018

1 reference

16 June 2018