Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy. [electronic resource]
Producer: 20141103Description: 782-8 p. digitalISSN:- 1552-4833
- Child Behavior Disorders -- diagnosis
- Child Development Disorders, Pervasive -- diagnosis
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 15
- Comparative Genomic Hybridization
- Epilepsy -- diagnosis
- Facies
- Haplotypes
- Humans
- Linkage Disequilibrium
- Male
- Pedigree
- Phenotype
- Polymorphism, Single Nucleotide
- Sialyltransferases -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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