Prenatal diagnosis of the 22q11.2 deletion syndrome. [electronic resource]
Producer: 20010927Description: 14-8 p. digitalISSN:- 1098-3600
- Abnormalities, Multiple
- Adult
- Chromosome Deletion
- Chromosomes, Human, Pair 22
- DiGeorge Syndrome -- diagnosis
- Facies
- Female
- Gene Deletion
- Genetic Counseling
- Humans
- In Situ Hybridization, Fluorescence -- methods
- Male
- Phenotype
- Polymerase Chain Reaction -- methods
- Prenatal Diagnosis
- Risk Factors
- Syndrome
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review
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