Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: a recognizable syndrome. [electronic resource]
Producer: 20050810Description: 76-80 p. digitalISSN:- 1552-4825
- Abnormalities, Multiple -- genetics
- Adolescent
- Adult
- Child
- Child, Preschool
- Chromosome Aberrations
- Chromosome Banding
- Chromosomes, Human, Pair 13 -- genetics
- Family Health
- Female
- Gene Duplication
- Genome, Human
- Genotype
- Hearing Loss -- pathology
- Humans
- In Situ Hybridization, Fluorescence
- Intellectual Disability -- pathology
- Karyotyping
- Male
- Middle Aged
- Nucleic Acid Hybridization -- methods
- Pedigree
- Phenotype
- Syndrome
- Tooth Abnormalities
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Publication Type: Comparative Study; Journal Article
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