Detection of constitutive cryptic chromosome aberrations;Diagnostik av medfødte kryptiske kromosomavvik

Tidsskrift for den Norske Laegeforening

Volumn 123, Issue 17, 2003, Pages 2418-2421

  Ness, Gro Oddveig ^a   Houge, Gunnar ^a  

^a Haukeland Universitetssykehus   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; DIAGNOSTIC AGENT;

CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME G BAND; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; DIAGNOSTIC ACCURACY; DNA SCREENING; EVALUATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENOME ANALYSIS; HUMAN; KARYOTYPING; MENTAL DEFICIENCY; MOLECULAR GENETICS; RELIABILITY; REVIEW; SCREENING TEST; SENSITIVITY AND SPECIFICITY; TECHNIQUE; TELOMERE; CHILD; CHROMOSOME DISORDER; COMPARATIVE STUDY; DEVELOPMENTAL DISORDER; DNA PROBE; GENETIC MARKER; GENETIC SCREENING; GENETICS; NUCLEIC ACID HYBRIDIZATION;

CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; DEVELOPMENTAL DISABILITIES; DNA PROBES; GENETIC MARKERS; GENETIC SCREENING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MENTAL RETARDATION; NUCLEIC ACID HYBRIDIZATION;

EID: 0642345016     PISSN: 00292001     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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