An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome. [electronic resource]
Producer: 20060810Description: 221-6 p. digitalISSN:- 1552-4825
- Abnormalities, Multiple -- genetics
- Chromosomes, Human, X -- genetics
- Face -- abnormalities
- Humans
- In Situ Hybridization, Fluorescence
- Intellectual Disability -- genetics
- Male
- Microsatellite Repeats -- genetics
- Microtubule-Associated Proteins -- genetics
- Nucleic Acid Hybridization -- genetics
- Pedigree
- Sex Chromosome Aberrations
- Sex Chromosome Disorders -- genetics
- Transcription Factors -- genetics
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Publication Type: Case Reports; Journal Article
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