A review of vascular anomalies: genetics and common syndromes.

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A review of vascular anomalies: genetics and common syndromes.

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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2014年學術文章

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A review of vascular anomalies: genetics and common syndromes.

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A review of vascular anomalies: genetics and common syndromes.

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A review of vascular anomalies: genetics and common syndromes.

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P1476

A review of vascular anomalies: genetics and common syndromes.

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P2093

Edward I Lee

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Elizabeth Killion

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Kriti Mohan

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P2860

Endoglin is an accessory protein that interacts with the signaling receptor complex of multiple members of the transforming growth factor-beta superfamily

Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome

Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2

Identification of human activin and TGF beta type I receptors that form heteromeric kinase complexes with type II receptors

Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype

Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations

A mosaic activating mutation in AKT1 associated with the Proteus syndrome

Is the E133K allele of VG5Q associated with Klippel-Trenaunay and other overgrowth syndromes?

Hereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesis

The G397A (E133K) change in the AGGF1 (VG5Q) gene is a single nucleotide polymorphism in the Spanish population

P304

64-68

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P31

scholarly article

P356

10.1055/S-0034-1376261

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P433

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

P478

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P577

2014-05-01T00:00:00Z

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P698

25045331

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P932

4078216

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