Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease (Q72155877)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7716719%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

title

Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7716719%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

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multiple endocrine neoplasia type 2A

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inferred from title

Hirschsprung's disease

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1

M J Borst

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author name string

J M VanCamp

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7716719%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

M L Peacock

series ordinal

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7716719%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

R A Decker

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7716719%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

language of work or name

1 reference

1 April 1995

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7716719%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

number of pages

6

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inferred from page(s)

published in

Surgery

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24 October 2019

volume

117

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24 October 2019

issue

4

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24 October 2019

page(s)

386-391

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

24 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

Hirschsprung's disease in a family with multiple endocrine neoplasia type 2.

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

Provocative agents and the diagnosis of medullary carcinoma of the thyroid gland

1 reference

https://api.crossref.org/works/10.1016%2FS0039-6060%2805%2980057-1

7 January 2021

10.1016/S0039-6060(05)80057-1

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7716719%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

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