(Q40479876)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

review article

1 reference

title

Hereditary tumor syndromes of the nervous system: overview and rare syndromes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

author name string

Louis DN

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

publication date

1 April 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

volume

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

page(s)

145-151

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

Cowden syndrome and Lhermitte-Duclos disease

23 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Bilateral retinoblastoma with ectopic intracranial retinoblastoma: trilateral retinoblastoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

TP53 Gene Mutations and 17p Deletions in Human Astrocytomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Genetic events in the development of Wilms' tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Mutations of the RET proto-oncogene in Hirschsprung's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Mortality from second tumors among long-term survivors of retinoblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

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/10.1111%2FJ.1750-3639.1995.TB00588.X

Functional inactivation of genes by dominant negative mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Exon scanning for mutation of the NF2 gene in schwannomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

A familial syndrome with cutaneous malignant melanoma and cerebral astrocytoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Mutation and cancer: statistical study of retinoblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Germline p53 gene mutations in subsets of glioma patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Turcot's syndrome: evidence for linkage to the adenomatous polyposis coli (APC) locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Association between meningioma and Cowden's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

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/10.1111%2FJ.1750-3639.1995.TB00588.X

Germ-line and somatic mutations of the APC gene in patients with Turcot syndrome and analysis of APC mutations in brain tumors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Genetic evidence that Turcot syndrome is not allelic to familial adenomatous polyposis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1995.TB00588.X

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/10.1111%2FJ.1750-3639.1995.TB00588.X

10.1111/J.1750-3639.1995.TB00588.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670655%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference