Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

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Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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2018年學術文章

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Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

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Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

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Item

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Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

@en

Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

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Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

@en

Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

@nl

P1476

Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes

@en

P2093

Cecilia W Lo

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George C Gabriel

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Gregory J Pazour

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P2860

Role of TBX1 in human del22q11.2 syndrome

Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome

Genetics and biology of primary ciliary dyskinesia

22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features

Global genetic analysis in mice unveils central role for cilia in congenital heart disease

New frontiers: discovering cilia-independent functions of cilia proteins

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies

Mutations in GRIP1 cause Fraser syndrome

Cardiovascular, skeletal, and renal defects in mice with a targeted disruption of the Pkd1 gene

P304

175

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scholarly article

P356

10.3389/FPED.2018.00175

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P478

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P577

2018-06-15T00:00:00Z

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29963541

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P932

6013576

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