Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies. [electronic resource]
Producer: 20070926Description: 697-709 p. digitalISSN:- 0340-6717
- Abnormalities, Multiple -- genetics
- Child
- Chromosome Aberrations
- Chromosome Breakage
- Chromosomes, Human, Pair 17 -- genetics
- Cytogenetics
- DNA -- genetics
- Female
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Infant, Newborn
- Male
- Nucleic Acid Hybridization
- Oligonucleotide Array Sequence Analysis
- Pregnancy
- Repetitive Sequences, Nucleic Acid
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Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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