Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family. [electronic resource]
Producer: 19990422Description: 141-8 p. digitalISSN:- 0888-7543
- Alopecia -- congenital
- Base Sequence
- Consanguinity
- DNA -- chemistry
- DNA Mutational Analysis
- Exons
- Family Health
- Female
- Gene Expression Regulation, Developmental
- Genes -- genetics
- Genotype
- Humans
- Introns
- Israel
- Male
- Molecular Sequence Data
- Mutation
- Pedigree
- Proteins -- genetics
- RNA, Messenger -- genetics
- Sequence Analysis, DNA
- Tissue Distribution
- Transcription Factors
- Transcription, Genetic
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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