Uncovering recurrent microdeletion syndromes and subtelomeric deletions/duplications through non-selective application of a MLPA-based extended prenatal panel in routine prenatal diagnosis. [electronic resource]
Producer: 20110930Description: 571-7 p. digitalISSN:- 1097-0223
- Adult
- Chorionic Villi Sampling -- statistics & numerical data
- Chromosome Aberrations -- statistics & numerical data
- Chromosome Deletion
- Comparative Genomic Hybridization
- Diagnostic Tests, Routine -- methods
- Female
- Gene Duplication
- Humans
- Incidence
- Karyotyping
- Male
- Nucleic Acid Amplification Techniques -- methods
- Pregnancy
- Prenatal Diagnosis -- methods
- Recurrence
- Syndrome
- Telomere -- genetics
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Publication Type: Case Reports; Evaluation Study; Journal Article
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