Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPE. [electronic resource]
Producer: 20110506Description: 421-40 p. digitalISSN:- 1432-1203
- Chromosomes, Human, Pair 3 -- genetics
- Comparative Genomic Hybridization
- Dandy-Walker Syndrome -- complications
- Eye Proteins -- genetics
- Female
- Fibroblast Growth Factor 8 -- genetics
- Gene Deletion
- Gene Duplication
- Glycogen Synthase Kinase 3 -- genetics
- Glycogen Synthase Kinase 3 beta
- Haploinsufficiency
- Hedgehog Proteins -- genetics
- Holoprosencephaly -- classification
- Homeodomain Proteins -- genetics
- Humans
- Male
- Models, Genetic
- Nerve Tissue Proteins -- genetics
- Oligonucleotide Array Sequence Analysis
- Phenotype
- Homeobox Protein SIX3
No physical items for this record
Publication Type: Journal Article
There are no comments on this title.
Log in to your account to post a comment.