Use of amniocytes for prenatal diagnosis of 22q11.2 microdeletion syndrome: a feasibility study. [electronic resource]
Producer: 20100527Description: 438-42 p. digitalISSN:- 2542-5641
- Adult
- Amniocentesis
- Cell Cycle Proteins -- genetics
- Chromosome Deletion
- Chromosomes, Human, Pair 22 -- genetics
- Feasibility Studies
- Female
- Fetal Diseases -- genetics
- Gestational Age
- Histone Chaperones -- genetics
- Humans
- In Situ Hybridization, Fluorescence
- Pregnancy
- Pregnancy Outcome
- Prenatal Diagnosis
- Transcription Factors -- genetics
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Publication Type: Journal Article
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