Orthopedic Manifestations of Mobius Syndrome: Case Series and Survey Study

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Update on 13 Syndromes Affecting Craniofacial and Dental Structures.Moebius Syndrome with Hypoglossal Palsy, Syndactyly, Brachydactyly, and Anisometropic Amblyopia.

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Orthopedic Manifestations of Mobius Syndrome: Case Series and Survey Study

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2016 nî lūn-bûn

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2016年論文

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Orthopedic Manifestations of Mobius Syndrome: Case Series and Survey Study

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Orthopedic Manifestations of Mobius Syndrome: Case Series and Survey Study

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Orthopedic Manifestations of Mobius Syndrome: Case Series and Survey Study

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Orthopedic Manifestations of Mobius Syndrome: Case Series and Survey Study

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Craig Eberson

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David Booy

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Julia Katarincic

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Philip McClure

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P2860

Deletion of chromosome 13 in Moebius syndrome.

Three-generation pedigree of a Möbius syndrome variant with chromosome translocation

Moebius syndrome

Möbius syndrome redefined: a syndrome of rhombencephalic maldevelopment.

A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family

Möbius-like syndrome associated with a 1;2 chromosome translocation.

De novo mutations in PLXND1 and REV3L cause Möbius syndrome

Prenatal exposure to misoprostol and congenital anomalies: systematic review and meta-analysis.

Subclavian artery supply disruption sequence: hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies.

MCA/MR syndrome with oligodactyly and Möbius anomaly in first cousins: new syndrome or familial facial-limb disruption sequence?

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scholarly article

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10.1155/2016/9736723

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2016

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2016-02-08T00:00:00Z

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Orthopedic Manifestations of Mobius Syndrome: Case Series and Survey Study

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P2860

P2860

Orthopedic Manifestations of Mobius Syndrome: Case Series and Survey Study

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P1476

P2093

P2860

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