Hydrops fetalis--has there been a change in diagnostic spectrum and mortality? - Wikidata - awgldk - TriplyDB

Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

http://www.wikidata.org/entity/Q39875893

about

Non-immune hydrops: Qatar experience.Amniotic fluid amino acid levels in non-immune hydrops fetalis: a case-control study.Etiology of non-immune hydrops fetalis: An update

P2860

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P2860

Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

http://www.wikidata.org/entity/Q39875893

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

2010年论文

@zh

2010年论文

@zh-cn

name

Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

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Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

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type

label

Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

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Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

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prefLabel

Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

@en

Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

@nl

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P356

14767058.2010.483522

P1433

Journal of Maternal-Fetal and Neonatal Medicine

P1476

Hydrops fetalis--has there been a change in diagnostic spectrum and mortality?

@en

P2093

Boris Metze

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

Christoph Bührer

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

Christoph Czernik

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

Hans Proquitté

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P2860

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome

Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia

Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease

Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2

Detection of alpha-thalassemia-1 Southeast Asian type using real-time gap-PCR with SYBR Green1 and high resolution melting analysis.

Hydrops fetalis.

Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.

Recurrent fetal hydrops due to mucopolysaccharidoses type VII.

Severity of non-immune hydrops fetalis at birth continues to predict survival despite advances in perinatal care.

Hydrops fetalis: a retrospective review of cases reported to a large national database and identification of risk factors associated with death.

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258-263

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scholarly article

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10.3109/14767058.2010.483522

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2

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24

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2010-05-07T00:00:00Z

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20446894

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