Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation. [electronic resource]
Producer: 20070716Description: 658-63 p. digitalISSN:- 1018-4813
- 5' Untranslated Regions -- genetics
- Adolescent
- Amino Acid Sequence
- Base Sequence
- Carrier State
- Child
- Chromosomes, Human, Pair 22 -- genetics
- DNA Mutational Analysis -- methods
- DiGeorge Syndrome -- genetics
- Female
- Gene Deletion
- Humans
- Infant, Newborn
- Intellectual Disability -- genetics
- Male
- Molecular Sequence Data
- Mutation, Missense
- Polymerase Chain Reaction -- methods
- T-Box Domain Proteins -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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