(Q74528947)

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11 November 2019

title

Severe Lhermitte-Duclos disease with unique germline mutation of PTEN (English)

1 reference

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11 November 2019

author name string

R Sutphen

1

1 reference

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11 November 2019

T M Diamond

2

1 reference

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11 November 2019

S E Minton

3

1 reference

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11 November 2019

M Peacocke

4

1 reference

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11 November 2019

H C Tsou

5

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11 November 2019

A W Root

6

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11 November 2019

publication date

1 February 1999

1 reference

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American Journal of Medical Genetics Part A

11 November 2019

published in

1 reference

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11 November 2019

volume

82

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11 November 2019

issue

4

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11 November 2019

page(s)

290-293

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Cowden syndrome and Lhermitte-Duclos disease

11 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990212%2982%3A4%3C290%3A%3AAID-AJMG3%3E3.0.CO%3B2-0

Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?

21 January 2018

1 reference

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Fine structure physical mapping of a 1.9 Mb region of chromosome 13q12.

21 January 2018

1 reference

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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/10.1002%2F%28SICI%291096-8628%2819990212%2982%3A4%3C290%3A%3AAID-AJMG3%3E3.0.CO%3B2-0

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis

21 January 2018

1 reference

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Germline mutations in PTEN are present in Bannayan-Zonana syndrome

21 January 2018

1 reference

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P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase

21 January 2018

1 reference

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Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.

21 January 2018

1 reference

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The cutaneous pathology of Cowden's disease: new findings

21 January 2018

1 reference

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The Cowden syndrome: a clinical and genetic study in 21 patients

21 January 2018

1 reference

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Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

21 January 2018

1 reference

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The genetic basis of Cowden's syndrome: three novel mutations in PTEN/MMAC1/TEP1.

21 January 2018

1 reference

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10.1002/(SICI)1096-8628(19990212)82:4<290::AID-AJMG3>3.0.CO;2-0

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10051160%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference