A novel immunodeficiency syndrome associated with partial trisomy 19p13. - Wikidata - awgldk - TriplyDB

A novel immunodeficiency syndrome associated with partial trisomy 19p13.

A novel immunodeficiency syndrome associated with partial trisomy 19p13.

http://www.wikidata.org/entity/Q37658726

about

Primary immunodeficiency associated with chromosomal aberration - an ESID survey Acne conglobata in a long-term survivor with trisomy 13, accompanied by selective IgM deficiency.

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A novel immunodeficiency syndrome associated with partial trisomy 19p13.

http://www.wikidata.org/entity/Q37658726

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

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scientific article published on 15 January 2014

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

A novel immunodeficiency syndrome associated with partial trisomy 19p13.

@en

A novel immunodeficiency syndrome associated with partial trisomy 19p13.

@nl

type

label

A novel immunodeficiency syndrome associated with partial trisomy 19p13.

@en

A novel immunodeficiency syndrome associated with partial trisomy 19p13.

@nl

prefLabel

A novel immunodeficiency syndrome associated with partial trisomy 19p13.

@en

A novel immunodeficiency syndrome associated with partial trisomy 19p13.

@nl

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JMEDGENET-2013-102122

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Journal of Medical Genetics

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A novel immunodeficiency syndrome associated with partial trisomy 19p13

@en

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Anette Schwerin-Nagel

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

Celia Duerr

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Christian Urban

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Elisangela Santos-Valente

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Jürgen Neesen

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Kaan Boztug

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Kambis Sadeghi

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Sabine Uhrig

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Stavroula Woutsas

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Winfried F Pickl

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P2860

Molecular and biological characterization of a ligand for CD27 defines a new family of cytokines with homology to tumor necrosis factor

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

E2A basic helix-loop-helix transcription factors in human leukemia

Plasma cell generation from B-lymphocytes via CD27/CD70 interaction.

The 22q11.2 deletion syndrome.

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

Syndromic immunodeficiencies: genetic syndromes associated with immune abnormalities.

CD27 deficiency is associated with combined immunodeficiency and persistent symptomatic EBV viremia

Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency.

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254-263

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scholarly article

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10.1136/JMEDGENET-2013-102122

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4

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Markus G. Seidel

Elisabeth Förster-Waldl

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2014-01-15T00:00:00Z

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259767768

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