[Detection of mosaic trisomy 9 missed by conventional cytogenetics using SNP-array and fluorescence in situ hybridization]. [electronic resource]
Producer: 20141006Description: 469-71 p. digitalISSN:- 1003-9406
- Adult
- Chromosomes, Human, Pair 9 -- genetics
- Female
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Male
- Mosaicism -- embryology
- Oligonucleotide Array Sequence Analysis -- instrumentation
- Polymorphism, Single Nucleotide
- Pregnancy
- Prenatal Diagnosis
- Trisomy -- diagnosis
- Uniparental Disomy -- cytology
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Publication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't
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