TY  - GEN
AU  - Jalali,Ali
AU  - Aldinger,Kimberly A
AU  - Chary,Ajit
AU  - McLone,David G
AU  - Bowman,Robin M
AU  - Le,Luan Cong
AU  - Jardine,Phillip
AU  - Newbury-Ecob,Ruth
AU  - Mallick,Andrew
AU  - Jafari,Nadereh
AU  - Russell,Eric J
AU  - Curran,John
AU  - Nguyen,Pam
AU  - Ouahchi,Karim
AU  - Lee,Charles
AU  - Dobyns,William B
AU  - Millen,Kathleen J
AU  - Pina-Neto,Joao M
AU  - Kessler,John A
AU  - Bassuk,Alexander G
TI  - Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity
SN  - 1432-1203
PY  - 2008///0422
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 2
KW  - genetics
KW  - Dandy-Walker Syndrome
KW  - complications
KW  - Encephalocele
KW  - Female
KW  - Genes, Dominant
KW  - Genetic Heterogeneity
KW  - Genetic Linkage
KW  - Genome, Human
KW  - Genotype
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Male
KW  - Nucleic Acid Hybridization
KW  - Occipital Bone
KW  - abnormalities
KW  - Pedigree
KW  - Polymorphism, Single Nucleotide
N1  - Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, N.I.H., Extramural
UR  - https://doi.org/10.1007/s00439-008-0467-y
ER  -