(Q57694734)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8673088%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

title

Localization of the gene for Cowden disease to chromosome 10q22-23 (English)

1 reference

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16 October 2019

11

1 reference

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16 October 2019

10

Easton DF

1 reference

16 October 2019

Nelen MR

1

1 reference

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16 October 2019

Padberg GW

2

1 reference

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16 October 2019

Peeters EA

3

1 reference

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16 October 2019

Lin AY

4

1 reference

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16 October 2019

van den Helm B

5

1 reference

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16 October 2019

Frants RR

6

1 reference

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16 October 2019

Coulon V

7

1 reference

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16 October 2019

Goldstein AM

8

1 reference

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16 October 2019

van Reen MM

9

1 reference

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16 October 2019

Hodgsen S

12

1 reference

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16 October 2019

Mulvihill JJ

13

1 reference

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16 October 2019

Murday VA

14

1 reference

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16 October 2019

Tucker MA

15

1 reference

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16 October 2019

Mariman EC

16

1 reference

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16 October 2019

Starink TM

17

1 reference

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16 October 2019

Ponder BA

18

1 reference

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16 October 2019

Ropers HH

19

1 reference

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16 October 2019

Kremer H

20

1 reference

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16 October 2019

Longy M

21

1 reference

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16 October 2019

Eng C

22

1 reference

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16 October 2019

language of work or name

English

0 references

publication date

1 May 1996

1 reference

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16 October 2019

1 reference

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16 October 2019

volume

13

1 reference

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16 October 2019

issue

1

1 reference

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16 October 2019

page(s)

114-116

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https://scigraph.springernature.com/pub.10.1038/ng0596-114

16 October 2019

exact match

0 references

cites work

Cowden's disease. A possible new symptom complex with multiple system involvement

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

The dermatopathology of Cowden's syndrome*

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

The cutaneous pathology of Cowden's disease: new findings

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Lhermitte-duclos disease and cowden disease: A single phakomatosis

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Cowden syndrome and Lhermitte-Duclos disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Cowden's disease with extensive gastrointestinal polyposis

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Allelotyping of follicular thyroid tumors

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Allelotype of uterine cancer by analysis of RFLP and microsatellite polymorphisms: frequent loss of heterozygosity on chromosome arms 3p, 9q, 10q, and 17p.

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Sequence-specific DNA-binding activities of the gap proteins encoded by hunchback and Krüppel in Drosophila

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Multiple zinc finger forms resulting from developmentally regulated alternative splicing of a transcription factor gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Transcriptional repression by YY1, a human GLI-Krüppel-related protein, and relief of repression by adenovirus E1A protein

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Competition for overlapping sites in the regulatory region of the Drosophila gene Krüppel.

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Discussion: genetics of multiple primary tumors: a clinical etiologic approach illustrated by three patients

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Localization of the gene for dominant cystoid macular dystrophy on chromosome 7p

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-114

7 January 2021

Identifiers

DOI

10.1038/NG0596-114

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8673088%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

1 reference