Diagnosing Chromosomal Abnormalities From "Big" to "Small" With Molecular Cytogenetic Technology

Journal of Obstetrics and Gynaecology Canada

Volumn 31, Issue 5, 2009, Pages 414-421

  Douglas Wilson, R ^a,d   Blight, Claire ^b   Langlois, Sylvie ^c  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b Reproductive Care Program of Nova Scotia   (Canada)

^c UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^d UNIVERSITY OF CALGARY   (Canada)

Author keywords

Chromosome abnormalities; Chromosome deletion syndromes; Prenatal diagnosis; Prenatal molecular cytogentic techniques; Ultrasound fetal anomalies

Indexed keywords

ANEUPLOIDY; ARTICLE; BALANCED TRANSLOCATION; CHROMOSOMAL MICRODELETION SYNDROME; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DIAGNOSTIC PROCEDURE; DIAGNOSTIC VALUE; DNA SEQUENCE; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENE SEQUENCE; GIEMSA BANDING TECHNIQUE; HUMAN; KARYOTYPE; KARYOTYPING; MICROARRAY ANALYSIS; MOLECULAR CLONING; MOLECULAR CYTOGENETIC TECHNOLOGY; MOLECULAR DIAGNOSIS; MORBIDITY; POSTNATAL MORBIDITY; PRENATAL DIAGNOSIS; ROBERTSONIAN CHROMOSOME TRANSLOCATION; FEMALE; METHODOLOGY; PREGNANCY; REVIEW;

CHROMOSOME ABERRATIONS; CYTOGENETIC ANALYSIS; FEMALE; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 70249103874     PISSN: 17012163     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1701-2163(16)34172-X     Document Type: Article

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