Discordant phenotype in monozygotic twins with renal coloboma syndrome and a PAX2 mutation. [electronic resource]
Producer: 20130124Description: 1989-93 p. digitalISSN:- 1432-198X
- Amino Acid Substitution
- Child, Preschool
- Coloboma -- diagnosis
- Cysteine
- Disease Progression
- Diseases in Twins -- diagnosis
- Environment
- Female
- Genetic Predisposition to Disease
- Heterozygote
- Humans
- Mutation
- PAX2 Transcription Factor -- genetics
- Phenotype
- Renal Insufficiency -- diagnosis
- Risk Factors
- Twins, Monozygotic -- genetics
- Vesico-Ureteral Reflux -- diagnosis
- Young Adult
No physical items for this record
Publication Type: Case Reports; 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.