Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis. [electronic resource]
Producer: 20000327Description: 138-43 p. digitalISSN:- 0197-3851
- Amniocentesis
- Chromosome Aberrations
- Chromosomes, Human, Pair 12
- Chromosomes, Human, Pair 15
- Chromosomes, Human, Pair 18
- Female
- Genetic Markers
- Humans
- In Situ Hybridization, Fluorescence
- Isochromosomes
- Male
- Pregnancy
- RNA, Long Noncoding
- RNA, Untranslated
- Sex Chromosome Aberrations
- Transcription Factors -- genetics
- Turner Syndrome -- diagnosis
- X Chromosome
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Publication Type: Journal Article
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