Early prenatal diagnosis of ICF syndrome by mutation detection

Prenatal Diagnosis

Volumn 27, Issue 11, 2007, Pages 1075-1078

  Rigolet, Muriel ^a,b   Grégoire, Annie ^a,b   Lefort, Geneviève ^c   Blanchet, Patricia ^c   Courbes, Christine ^c   Rodìere, Michel ^c   Sarda, Pierre ^c   Viegas Péquignot, Evani ^a,b  

^a INSERM   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

^c HÔPITAL ARNAUD DE VILLENEUVE   (France)

Author keywords

DNMT3B; Heterochromatin; ICF syndrome; Methylation; Prenatal diagnosis

Indexed keywords

ACUTE APPENDICITIS; ADULT; ARTICLE; BACTERIAL PERITONITIS; BRAIN ATROPHY; BRONCHOPATHY; CANDIDIASIS; CARDIOMYOPATHY; CASE REPORT; CENTROMERIC INSTABILITY; FACE MALFORMATION; FEMALE; FETUS KARYOTYPING; FEVER; GENETIC COUNSELING; GENETIC DISORDER; HEPATOSPLENOMEGALY; HORSESHOE KIDNEY; HUMAN; HYPERTELORISM; HYPOGAMMAGLOBULINEMIA; ICF SYNDROME; IMMUNE DEFICIENCY; INFANTILE HYPOTONIA; MACROGLOSSIA; NEUTROPENIA; NUCLEOTIDE SEQUENCE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SALMONELLOSIS; SEPTICEMIA; VIRUS MENINGITIS;

ABNORMALITIES, MULTIPLE; CENTROMERE; CONSANGUINITY; CYTOGENETIC ANALYSIS; DNA (CYTOSINE-5-)-METHYLTRANSFERASE; DNA METHYLATION; DNA MUTATIONAL ANALYSIS; EARLY DIAGNOSIS; FACIAL ASYMMETRY; FEMALE; GENOMIC INSTABILITY; HUMANS; INFANT; INFANT, NEWBORN; MALE; PEDIGREE; PREGNANCY; PRENATAL DIAGNOSIS; SYNDROME;

EID: 36148952889     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1826     Document Type: Article

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