Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disability. [electronic resource]
Producer: 20130909Description: 860-4 p. digitalISSN:- 1552-4833
- Abnormalities, Multiple -- diagnosis
- Child
- Chromosome Deletion
- Chromosomes, Human, X
- Coenzyme A Ligases -- genetics
- Facies
- Gene Deletion
- Genome-Wide Association Study
- Genotype
- Humans
- In Situ Hybridization, Fluorescence
- Intellectual Disability -- genetics
- Male
- Phenotype
- Polymorphism, Single Nucleotide
- Long-Chain-Fatty-Acid-CoA Ligase
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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