Molecular karyotyping as a relevant diagnostic tool in children with growth retardation with Silver-Russell features. [electronic resource]
Producer: 20130110Description: 933-42 p. digitalISSN:- 1097-6833
- Child
- Child, Preschool
- Chromosome Aberrations
- Chromosome Deletion
- Chromosomes, Human, Pair 11 -- genetics
- Chromosomes, Human, Pair 7 -- genetics
- Female
- Genetic Markers -- genetics
- Growth Disorders -- diagnosis
- Humans
- Infant
- Karyotyping -- methods
- Male
- Mutation
- Oligonucleotide Array Sequence Analysis
- Phenotype
- Polymorphism, Single Nucleotide
- Silver-Russell Syndrome -- diagnosis
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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