A patient with MEN1 typical features and MEN2-like features. - Wikidata - awgldk - TriplyDB

A patient with MEN1 typical features and MEN2-like features.

A patient with MEN1 typical features and MEN2-like features.

http://www.wikidata.org/entity/Q37226787

about

MEN4 and CDKN1B mutations: the latest of the MEN syndromes.

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A patient with MEN1 typical features and MEN2-like features.

http://www.wikidata.org/entity/Q37226787

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 08 April 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

A patient with MEN1 typical features and MEN2-like features.

@en

A patient with MEN1 typical features and MEN2-like features.

@nl

type

label

A patient with MEN1 typical features and MEN2-like features.

@en

A patient with MEN1 typical features and MEN2-like features.

@nl

prefLabel

A patient with MEN1 typical features and MEN2-like features.

@en

A patient with MEN1 typical features and MEN2-like features.

@nl

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International journal of endocrine oncology

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A patient with MEN1 typical features and MEN2-like features.

@en

P2093

James Welch

http://www.w3.org/2001/XMLSchema#string

Lee S Weinstein

http://www.w3.org/2001/XMLSchema#string

Stephen J Marx

http://www.w3.org/2001/XMLSchema#string

William F Simonds

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P2860

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors

Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.

Functional collaboration between different cyclin-dependent kinase inhibitors suppresses tumor growth with distinct tissue specificity.

Causes of enlarged corneal nerves.

Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.

Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility.

Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.

The modifier role of RET-G691S polymorphism in hereditary medullary thyroid carcinoma: functional characterization and expression/penetrance studies.

Multiple orbital neurofibromas, painful peripheral nerve tumors, distinctive face and marfanoid habitus: a new syndrome.

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89-95

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scholarly article

P356

10.2217/IJE-2015-0008

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2

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3

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Sunita K Agarwal

Diala El-Maouche

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2016-04-08T00:00:00Z

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27594983

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5008851

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