From karyotyping to array-CGH in prenatal diagnosis

Cytogenetic and Genome Research

Volumn 135, Issue 3-4, 2011, Pages 241-250

  Lichtenbelt, K D ^a   Knoers, N V A M ^a   Schuring Blom, G H ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

Array; Chromosomal anomaly; Comparative genomic hybridization; Karyotyping; Prenatal diagnosis

Indexed keywords

ARTICLE; CHROMOSOME ABERRATION; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL MALFORMATION; FEMALE; FETUS ECHOGRAPHY; HUMAN; INTELLECTUAL IMPAIRMENT; KARYOTYPING; MICROARRAY ANALYSIS; PATIENT COUNSELING; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RETROSPECTIVE STUDY;

CHROMOSOME ABERRATIONS; COMPARATIVE GENOMIC HYBRIDIZATION; DIAGNOSTIC ERRORS; FEMALE; HUMANS; KARYOTYPING; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PREGNANCY; PRENATAL DIAGNOSIS; SENSITIVITY AND SPECIFICITY;

EID: 83555168187     PISSN: 14248581     EISSN: 14219794     Source Type: Journal    
DOI: 10.1159/000334065     Document Type: Article

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