Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosis. [electronic resource]
Producer: 19940209Description: 825-32 p. digitalISSN:- 0197-3851
- Adult
- Amniocentesis
- Chromosome Aberrations -- diagnosis
- Chromosome Banding
- Chromosome Disorders
- Chromosomes, Human, Pair 11
- Chromosomes, Human, Pair 15
- Chromosomes, Human, Pair 18
- DNA Probes
- Dandy-Walker Syndrome -- diagnosis
- Female
- Fetal Diseases -- diagnosis
- Humans
- In Situ Hybridization, Fluorescence -- methods
- Infant, Newborn
- Karyotyping
- Pregnancy
- Pregnancy Trimester, Second
- Pregnancy Trimester, Third
- Prenatal Diagnosis -- methods
- Translocation, Genetic
- Trisomy
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Publication Type: Case Reports; Journal Article
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