Intrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20. [electronic resource]
Producer: 20080227Description: 288-93 p. digitalISSN:- 1552-4825
- Abnormalities, Multiple -- diagnosis
- Child
- Child, Preschool
- Chromosome Breakage
- Chromosome Inversion
- Chromosomes, Human, Pair 20 -- genetics
- Cryptorchidism -- diagnosis
- Diagnosis, Differential
- Epilepsy -- diagnosis
- Genetic Markers
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Karyotyping
- Male
- Microcephaly -- diagnosis
- Recombination, Genetic
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Publication Type: Case Reports; Journal Article
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