TY  - GEN
AU  - Rigolet,Muriel
AU  - Grégoire,Annie
AU  - Lefort,Geneviève
AU  - Blanchet,Patricia
AU  - Courbes,Christine
AU  - Rodière,Michel
AU  - Sarda,Pierre
AU  - Viegas-Péquignot,Evani
TI  - Early prenatal diagnosis of ICF syndrome by mutation detection
SN  - 0197-3851
PY  - 2008///0211
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Centromere
KW  - genetics
KW  - Consanguinity
KW  - Cytogenetic Analysis
KW  - DNA (Cytosine-5-)-Methyltransferases
KW  - DNA Methylation
KW  - DNA Mutational Analysis
KW  - Early Diagnosis
KW  - Facial Asymmetry
KW  - congenital
KW  - Female
KW  - Genomic Instability
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Pedigree
KW  - Pregnancy
KW  - Prenatal Diagnosis
KW  - methods
KW  - Syndrome
KW  - DNA Methyltransferase 3B
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/pd.1826
ER  -