Rare deleterious variants in GRHL3 are associated with human spina bifida.

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Grainyhead-like Transcription Factors in Craniofacial Development.Mis-expression of grainyhead-like transcription factors in zebrafish leads to defects in enveloping layer (EVL) integrity, cellular morphogenesis and axial extension.

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Rare deleterious variants in GRHL3 are associated with human spina bifida.

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Rare deleterious variants in GRHL3 are associated with human spina bifida.

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label

Rare deleterious variants in GRHL3 are associated with human spina bifida.

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prefLabel

Rare deleterious variants in GRHL3 are associated with human spina bifida.

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P1476

Rare deleterious variants in GRHL3 are associated with human spina bifida.

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Alexandre Emond

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

Andrea Accogli

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

Elisa Merello

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

Patrizia De Marco

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Philippe Lemay

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

Sandra Laurent

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

Valeria Capra

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

Zoha Kibar

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P2860

Two isoforms of Sister-Of-Mammalian Grainyhead have opposing functions in endothelial cells and in vivo

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Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

Mutations in VANGL1 associated with neural-tube defects

Regional neural tube closure defined by the Grainy head-like transcription factors

Inositol- and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3

Grainyhead-like 2 regulates neural tube closure and adhesion molecule expression during neural fold fusion

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716-724

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scholarly article

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10.1002/HUMU.23214

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

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Guy A. Rouleau

Alexandre Dionne-Laporte

Dan Spiegelman

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2017-03-08T00:00:00Z

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28276201

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spina bifida

Rare deleterious variants in GRHL3 are associated with human spina bifida.

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P2860

P2860

Rare deleterious variants in GRHL3 are associated with human spina bifida.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921