Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion

被引:0
作者
Anudeep Yekula
Connor Grant
Mihir Gupta
David R. Santiago-Dieppa
Pate J. Duddleston
David Gonda
Michael Levy
机构
[1] Massachusetts General Hospital,Department of Neurosurgery
[2] University of California San Diego,Department of Neurosurgery
[3] Mercer University,School of Medicine
[4] Rady Children’s Hospital,Department of Pediatric Neurosurgery
来源
Child's Nervous System | 2020年 / 36卷
关键词
Pierre Robin sequence; Spine; Tethered cord; Deformity; Molecular genetics; Genomics; Molecular basis of disease;
D O I
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中图分类号
学科分类号
摘要
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页码:1367 / 1377
页数:10
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[3]  
Poets CF(2004)Pierre Robin sequence in Denmark: a retrospective population-based epidemiological study Cleft Palate Craniofac J 41 47-880
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Suri S(2016)Clinical, cytogenetic, and molecular outcomes in a series of 66 patients with Pierre Robin sequence and literature review: 22q11.2 deletion is less common than other chromosomal anomalies Am J Med Genet A 170A 870-259
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