Chiari Malformation Type I: A Case-Control Association Study of 58 Developmental Genes

Institutional experience with 500 cases of surgically treated pediatric Chiari malformation Type I

(2011) R. Shane Tubbs et al.   Journal of Neurosurgery-Pediatrics

Familial Chiari malformation: case series

(2011) Benjamin D. Schanker et al.   Neurosurgical Focus

Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management

(2010) Thomas H. Milhorat et al.   ACTA NEUROCHIRURGICA

Rubinstein-Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: A contiguous gene syndrome?

(2010) Cezary Wójcik et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Hox Genes and Segmentation of the Hindbrain and Axial Skeleton

(2009) Tara Alexander et al.   Annual Review of Cell and Developmental Biology

Genetics of human neural tube defects

(2009) N. D.E. Greene et al.   HUMAN MOLECULAR GENETICS

Incidence of basioccipital hypoplasia in Chiari malformation Type I: comparative morphometric study of the posterior cranial fossa

(2009) Rémy Noudel et al.   JOURNAL OF NEUROSURGERY

Rhythmic gene expression in somite formation and neural development

(2009) Ryoichiro Kageyama et al.   MOLECULES AND CELLS

SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies

(2009) Zongli Xu et al.   NUCLEIC ACIDS RESEARCH

Abnormal Basiocciput Development in CHARGE Syndrome

(2008) K. Fujita et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

Retinoic Acid Synthesis and Signaling during Early Organogenesis

(2008) Gregg Duester   CELL

Retinoic acid in development: towards an integrated view

(2008) Karen Niederreither et al.   NATURE REVIEWS GENETICS