MSX2 Gene Duplication in a Patient with Eye Development Defects.

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A Genetic-Pathophysiological Framework for Craniosynostosis

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Q26784240-91E68E6C-3BD6-475B-BC72-725DC26524CA

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MSX2 Gene Duplication in a Patient with Eye Development Defects.

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MSX2 Gene Duplication in a Patient with Eye Development Defects.

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MSX2 Gene Duplication in a Patient with Eye Development Defects.

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MSX2 Gene Duplication in a Patient with Eye Development Defects.

@en

MSX2 Gene Duplication in a Patient with Eye Development Defects.

@nl

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MSX2 Gene Duplication in a Patient with Eye Development Defects.

@en

MSX2 Gene Duplication in a Patient with Eye Development Defects.

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P1476

MSX2 Gene Duplication in a Patient with Eye Development Defects

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P2093

Claude Speeg-Schatz

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Elisabeth Flori

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Elise Schaefer

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Fouzia Studer

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Hélène Dollfus

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Julie Plaisancié

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Mélanie Fradin

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Valerie Pelletier

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Yaumara Perdomo

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P2860

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

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Msx1 and Msx2 in limb mesenchyme modulate digit number and identity

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Enamel protein regulation and dental and periodontal physiopathology in MSX2 mutant mice

Msx homeobox gene family and craniofacial development.

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353-358

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scholarly article

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10.3109/13816810.2014.886270

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P433

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P478

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Corinne Collet

A Bloch-Zupan

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2014-03-25T00:00:00Z

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P698

24666290

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MSX2 Gene Duplication in a Patient with Eye Development Defects.

about

P2860

P2860

MSX2 Gene Duplication in a Patient with Eye Development Defects.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698