Chromosome 5q33 deletions associated with congenital heart defects.

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Chromosome 5q33 deletions associated with congenital heart defects.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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Chromosome 5q33 deletions associated with congenital heart defects.

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Chromosome 5q33 deletions associated with congenital heart defects.

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Chromosome 5q33 deletions associated with congenital heart defects.

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Chromosome 5q33 deletions associated with congenital heart defects.

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Chromosome 5q33 deletions associated with congenital heart defects.

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Chromosome 5q33 deletions associated with congenital heart defects.

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P1476

Chromosome 5q33 deletions associated with congenital heart defects.

@en

P2093

Catherine L Mercer

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Daryl A Scott

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Molly Starkovich

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Seema R Lalani

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P2860

TGF-beta induces the expression of SAP30L, a novel nuclear protein

A functional genetic study identifies HAND1 mutations in septation defects of the human heart

A loss-of-function mutation in the binding domain of HAND1 predicts hypoplasia of the human hearts

SAP30L interacts with members of the Sin3A corepressor complex and targets Sin3A to the nucleolus

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

Analysis of protein-coding genetic variation in 60,706 humans

The Hand1 and Hand2 transcription factors regulate expansion of the embryonic cardiac ventricles in a gene dosage-dependent manner

Homeodomain factor Nkx2-5 controls left/right asymmetric expression of bHLH gene eHand during murine heart development

The Hand1 bHLH transcription factor is essential for placentation and cardiac morphogenesis

The bHLH factors, dHAND and eHAND, specify pulmonary and systemic cardiac ventricles independent of left-right sidedness

P304

3338-3342

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P31

scholarly article

P356

10.1002/AJMG.A.37957

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P407

English

P433

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P478

170

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P577

2016-09-02T00:00:00Z

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P698

27589475

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