Mutations of the RET proto-oncogene in Hirschsprung's disease (Q24324643)

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

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instance of

scholarly article

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title

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

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main subject

ret proto-oncogene

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stated in

GOA release 2020-03-11

posterior midgut development

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stated in

GOA release 2020-03-11

Hirschsprung's disease

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based on heuristic

inferred from title

author

Arnold Munnich

series ordinal

10

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Stanislas Lyonnet

object named as

S Lyonnet

series ordinal

2

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author name string

P Edery

series ordinal

1

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L M Mulligan

series ordinal

3

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A Pelet

series ordinal

4

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E Dow

series ordinal

5

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L Abel

series ordinal

6

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S Holder

series ordinal

7

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C Nihoul-Fékété

series ordinal

8

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B A Ponder

series ordinal

9

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language of work or name

English

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publication date

27 January 1994

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published in

Nature

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volume

367

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issue

6461

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page(s)

378-80

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cites work

Adult-Onset Hirschsprung's Disease

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Myenteric plexus in congenital megacolon; study of 11 cases

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

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Three-generation transmission of Hirschsprung's disease

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

MONGOLISM ASSOCIATED WITH HIRSCHSPRUNG'S DISEASE

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of Megacolon with Two Recessive Spotting Genes in the Mouse

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

How sensitive is PCR-SSCP?

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The human protooncogene ret: a communicative cadherin?

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F367378A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/367378A0

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3840761

Dimensions Publication ID

1040357518

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Fatcat ID

release_euhfumf5vngq7b32e6y4voirta

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OpenCitations bibliographic resource ID

3840761

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3840761

PubMed publication ID

8114939

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3840761

 

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