Population-based description of familial clustering of Chiari malformation Type I

Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics

(2014) Christina A Markunas et al.   BMC Medical Genomics

Genetic Evaluation and Application of Posterior Cranial Fossa Traits as Endophenotypes for Chiari Type I Malformation

(2013) Christina A. Markunas et al.   ANNALS OF HUMAN GENETICS

Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates

(2013) Christina A. Markunas et al.   PLoS One

Familial Chiari malformation: case series

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

Chiari Type I Malformation in a Pediatric Population

(2009) Leslie A. Aitken et al.   PEDIATRIC NEUROLOGY

Spontaneous resolution of Chiari malformation Type I in monozygotic twins

(2008) Jeffrey H. Miller et al.   Journal of Neurosurgery-Pediatrics