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Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype.The rare sprengel deformity: our experience with three casesSprengel's deformity and spinal dysraphism: connecting the shoulder and the spine.Dysphagia associated with cervical spine and postural disorders.A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel's deformity.Malformed vertebrae: a clinical and imaging review.Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome.A skeletal disorder in a dog resembling the Klippel-Feil Syndrome with Sprengel's Deformity in humans.
P2860
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P2860
description
article científic
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article scientifique
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articol științific
@ro
articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
@id
artikull shkencor
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artículo científico
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name
Sprengel deformity: pathogenesis and management.
@en
Sprengel deformity: pathogenesis and management.
@nl
type
label
Sprengel deformity: pathogenesis and management.
@en
Sprengel deformity: pathogenesis and management.
@nl
prefLabel
Sprengel deformity: pathogenesis and management.
@en
Sprengel deformity: pathogenesis and management.
@nl
P2093
P356
P1476
Sprengel deformity: pathogenesis and management
@en
P2093
Jean A Ouellet
Mitchell Bernstein
Neil Saran
Nicholas M Desy
P304
P356
10.5435/JAAOS-20-03-177
P577
2012-03-01T00:00:00Z