The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis

Prenatal Diagnosis

Volumn 25, Issue 11, 2005, Pages 1057-1058

  Milunsky, A ^a   Konialis, C ^b   Shim, S H ^a   Maher, T A ^a   Spengos, K ^c   Ito, M ^a   Pangalos, C ^b  

^a BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Diagnostic Genetic Center   (Greece)

^c UNIVERSITY OF ATHENS   (Greece)

Author keywords

CADASIL; Dementia; Notch3 gene; Prenatal diagnosis; Stroke

Indexed keywords

NOTCH3 RECEPTOR;

ARTICLE; BRAIN ISCHEMIA; CADASIL; CASE REPORT; COGNITIVE DEFECT; DISEASE COURSE; FETUS; GENE MUTATION; GENETIC DISORDER; HUMAN; MULTIINFARCT DEMENTIA; MUTAGENESIS; MUTATIONAL ANALYSIS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; STROKE; VASCULAR DISEASE;

ABORTION, EUGENIC; ADULT; CADASIL; DNA MUTATIONAL ANALYSIS; FEMALE; FETAL DISEASES; GENES, DOMINANT; HUMANS; MALE; MUTATION; PREGNANCY; PRENATAL DIAGNOSIS; RECEPTORS, NOTCH;

EID: 28544447923     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1302     Document Type: Article

References (8)

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