Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. [electronic resource]
Producer: 20080422Description: 237-45 p. digitalISSN:- 1432-1203
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 2 -- genetics
- Dandy-Walker Syndrome -- complications
- Encephalocele -- complications
- Female
- Genes, Dominant
- Genetic Heterogeneity
- Genetic Linkage -- genetics
- Genome, Human
- Genotype
- Humans
- In Situ Hybridization, Fluorescence
- Male
- Nucleic Acid Hybridization
- Occipital Bone -- abnormalities
- Pedigree
- Polymorphism, Single Nucleotide -- genetics
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Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, N.I.H., Extramural
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