Cervical artery dissection expands the cardiovascular phenotype in FBN1-related Weill-Marchesani syndrome.

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Cervical artery dissection expands the cardiovascular phenotype in FBN1-related Weill-Marchesani syndrome.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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name

Cervical artery dissection exp ...... ted Weill-Marchesani syndrome.

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Cervical artery dissection exp ...... ted Weill-Marchesani syndrome.

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Item

label

Cervical artery dissection exp ...... ted Weill-Marchesani syndrome.

@en

Cervical artery dissection exp ...... ted Weill-Marchesani syndrome.

@nl

prefLabel

Cervical artery dissection exp ...... ted Weill-Marchesani syndrome.

@en

Cervical artery dissection exp ...... ted Weill-Marchesani syndrome.

@nl

P1476

Cervical artery dissection exp ...... ated Weill-Marchesani syndrome

@en

P2093

Angela Lin

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Brian Ghoshhajra

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Eric Isselbacher

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Mark E Lindsay

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Wendy Smith

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P2860

ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts.

ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome

In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome

Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome

LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma

Familial occurrence and heritable connective tissue disorders in cervical artery dissection

Marfan Database (third edition): new mutations and new routines for the software.

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias.

Atenolol versus losartan in children and young adults with Marfan's syndrome.

The etiology of cervical artery dissection.

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2551-2556

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scholarly article

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10.1002/AJMG.A.38353

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English

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173

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Kelsey Newell

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2017-07-11T00:00:00Z

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P698

28696036

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