CDKN1C mutations: two sides of the same coin. [electronic resource]
Producer: 20150723Description: 614-22 p. digitalISSN:- 1471-499X
- Adrenal Insufficiency -- diagnosis
- Animals
- Beckwith-Wiedemann Syndrome -- diagnosis
- Chromosome Aberrations
- Chromosomes, Human, Pair 11
- Cyclin-Dependent Kinase Inhibitor p57 -- genetics
- Disease Management
- Fetal Growth Retardation -- diagnosis
- Genetic Association Studies
- Genetic Counseling
- Genomic Imprinting
- Humans
- Mutation
- Osteochondrodysplasias -- diagnosis
- Urogenital Abnormalities -- diagnosis
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
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