[HOXD13 polyalanine tract expansion in synpolydactyly: mutation detection and prenatal diagnosis in a large Chinese family]. [electronic resource]
Producer: 20090319Description: 5-9 p. digitalISSN:- 1003-9406
- Base Sequence
- China
- DNA Mutational Analysis
- Family Health
- Female
- Homeodomain Proteins -- genetics
- Humans
- Male
- Molecular Sequence Data
- Mutation
- Pedigree
- Peptides -- genetics
- Polydactyly -- diagnosis
- Polymerase Chain Reaction
- Pregnancy
- Prenatal Diagnosis -- methods
- Transcription Factors -- genetics
- Trinucleotide Repeat Expansion
No physical items for this record
Publication Type: English Abstract; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.