Clinical, genetic and environmental factors associated with congenital vertebral malformations. - Wikidata - wikimedia - TriplyDB

Clinical, genetic and environmental factors associated with congenital vertebral malformations.

Clinical, genetic and environmental factors associated with congenital vertebral malformations.

http://www.wikidata.org/entity/Q36802361

about

The genetic landscape and clinical implications of vertebral anomalies in VACTERL association Congenital spinal gibbosity evoking Pott's disease in a newborn born to a tubercular mother: report of a case and review of the literature From dinosaurs to birds: a tail of evolution Reproductive Toxic Chemicals at Work and Efforts to Protect Workers' Health: A Literature Review.The Crossed Flexor Plantar Response in Patients with Klippel-Feil Syndrome Prevalence of Klippel-Feil Syndrome in a Surgical Series of Patients with Cervical Spondylotic Myelopathy: Analysis of the Prospective, Multicenter AOSpine North America Study.Proatlas segmentation anomalies: Surgical management of five cases and review of the literature.Progress and perspective of TBX6 gene in congenital vertebral malformations.Congenital Kyphoscoliosis in Monozygotic Twins: Ten-Year Follow-up Treated by Posterior Vertebral Column Resection (PVCR): A Case Report.Abnormal fetal muscle forces result in defects in spinal curvature and alterations in vertebral segmentation and shape.A case report of amyotrophic lateral sclerosis in a patient with Klippel-Feil syndrome—a familial occurrence: a potential role of TGF-β signaling pathway.Functional and In Silico Assessment of GDF3 Gene Variants in a Chinese Congenital Scoliosis Population.

P2860

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P2860

Clinical, genetic and environmental factors associated with congenital vertebral malformations.

http://www.wikidata.org/entity/Q36802361

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

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Clinical, genetic and environm ...... nital vertebral malformations.

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Clinical, genetic and environm ...... nital vertebral malformations.

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Clinical, genetic and environm ...... nital vertebral malformations.

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Clinical, genetic and environm ...... nital vertebral malformations.

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Clinical, genetic and environm ...... nital vertebral malformations.

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Molecular syndromology

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Clinical, genetic and environm ...... nital vertebral malformations.

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C L Raggio

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M A Pickart

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P F Giampietro

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P2860

Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome

Human genome sequencing in health and disease

Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

Mutated MESP2 causes spondylocostal dysostosis in humans.

Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype

Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis

Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome

Wildervanck's syndrome and mirror movements: a congenital disorder of axon migration?

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94-105

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10.1159/000345329

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1-2

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4

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Catherine A. McCarty

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