Early prenatal diagnosis of ICF syndrome by mutation detection. [electronic resource]
Producer: 20080211Description: 1075-8 p. digitalISSN:- 0197-3851
- Abnormalities, Multiple -- diagnosis
- Centromere -- genetics
- Consanguinity
- Cytogenetic Analysis
- DNA (Cytosine-5-)-Methyltransferases -- genetics
- DNA Methylation
- DNA Mutational Analysis
- Early Diagnosis
- Facial Asymmetry -- congenital
- Female
- Genomic Instability
- Humans
- Infant
- Infant, Newborn
- Male
- Pedigree
- Pregnancy
- Prenatal Diagnosis -- methods
- Syndrome
- DNA Methyltransferase 3B
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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