Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio. [electronic resource]
Producer: 20080128Description: 1225-35 p. digitalISSN:- 1098-1004
- Angelman Syndrome -- genetics
- Beckwith-Wiedemann Syndrome -- genetics
- Chromosome Deletion
- Female
- Genotype
- Humans
- In Situ Hybridization, Fluorescence
- Male
- Nuclear Family
- Polymorphism, Single Nucleotide -- genetics
- Prader-Willi Syndrome -- genetics
- Pseudohypoparathyroidism -- genetics
- Software
- Uniparental Disomy -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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