Immunodeficiency in patients with 49,XXXXY chromosomal variation. - Wikidata - wikimedia - TriplyDB

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

http://www.wikidata.org/entity/Q42750781

about

Primary immunodeficiency associated with chromosomal aberration - an ESID survey Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects.

P2860

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P2860

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

http://www.wikidata.org/entity/Q42750781

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

@en

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

@nl

type

label

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

@en

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

@nl

prefLabel

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

@en

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

@nl

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P1433

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

P1476

Immunodeficiency in patients with 49,XXXXY chromosomal variation

@en

P2093

Carole Samango-Sprouse

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

Michael D Keller

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

Teresa Sadeghin

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

P2860

48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome

Practice parameter for the diagnosis and management of primary immunodeficiency

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

Genome-wide association identifies diverse causes of common variable immunodeficiency

Infections and immunodeficiency in Down syndrome.

Inherited tandem duplication of the X chromosome: dup(X)(q13.2-q21.2) in a family.

Partial monosomy 22 as result of an X/22 translocation in a newborn with DiGeorge syndrome.

Study of autoimmunity in Klinefelter's syndrome and idiopathic hypogonadotropic hypogonadism.

Use and interpretation of diagnostic vaccination in primary immunodeficiency: a working group report of the Basic and Clinical Immunology Interest Section of the American Academy of Allergy, Asthma & Immunology.

Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome.

P304

50-54

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scholarly article

P356

10.1002/AJMG.C.31348

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P433

1

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163C

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2013-01-23T00:00:00Z

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235367819

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23345259

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4886306

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