Early prenatal diagnosis of ICF syndrome by mutation detection.

Rigolet, Muriel

Early prenatal diagnosis of ICF syndrome by mutation detection. [electronic resource] - Prenatal diagnosis Nov 2007 - 1075-8 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

0197-3851

10.1002/pd.1826 doi


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