Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome. [electronic resource]
Producer: 20110509Description: 360-4 p. digitalISSN:- 1546-1718
- Adolescent
- Amino Acid Sequence
- Base Sequence
- Cell Cycle Proteins -- genetics
- Child
- Child, Preschool
- Congenital Microtia
- Consanguinity
- Conserved Sequence
- DNA -- genetics
- Ear -- abnormalities
- Female
- Founder Effect
- Growth Disorders -- genetics
- Haplotypes
- Humans
- Male
- Micrognathism -- genetics
- Molecular Sequence Data
- Mutation
- Origin Recognition Complex -- genetics
- Patella -- abnormalities
- Pedigree
- Polymorphism, Single Nucleotide
- Sequence Homology, Amino Acid
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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