Localization of the gene for Cowden disease to chromosome 10q22–23 (Q57694734)

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16 October 2019

title

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

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Easton DF

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Nelen MR

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Padberg GW

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Peeters EA

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Lin AY

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van den Helm B

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Frants RR

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Goldstein AM

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van Reen MM

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Hodgsen S

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Mulvihill JJ

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Ponder BA

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Ropers HH

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Kremer H

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Longy M

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Eng C

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language of work or name

English

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publication date

1 May 1996

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16 October 2019

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volume

13

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issue

1

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page(s)

114-116

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

16 October 2019

exact match

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cites work

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

1 reference

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7 January 2021

The dermatopathology of Cowden's syndrome*

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7 January 2021

The cutaneous pathology of Cowden's disease: new findings

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7 January 2021

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

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7 January 2021

Lhermitte-duclos disease and cowden disease: A single phakomatosis

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7 January 2021

Cowden syndrome and Lhermitte-Duclos disease

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7 January 2021

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

1 reference

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7 January 2021

Cowden's disease with extensive gastrointestinal polyposis

1 reference

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7 January 2021

Allelotyping of follicular thyroid tumors

1 reference

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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

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7 January 2021

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

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Identifiers

DOI

10.1038/NG0596-114

1 reference

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16 October 2019

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