Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease. [electronic resource]
Producer: 19940331Description: 2099-107 p. digitalISSN:- 0964-6906
- Abnormalities, Multiple -- genetics
- Amino Acid Sequence
- Animals
- Base Sequence
- Cell Cycle Proteins
- Chromosome Mapping
- Chromosomes, Human, Pair 22
- Consensus Sequence
- DiGeorge Syndrome -- genetics
- Embryonic and Fetal Development
- Enhancer Elements, Genetic
- Genomic Library
- Heart Defects, Congenital -- genetics
- Histone Chaperones
- Humans
- In Situ Hybridization, Fluorescence
- Mice
- Molecular Sequence Data
- Multigene Family
- Polymerase Chain Reaction
- Sequence Deletion
- Sequence Homology, Amino Acid
- Transcription Factors -- genetics
- Transducin -- genetics
- Translocation, Genetic
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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