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Volumn 9, Issue 2, 2007, Pages 277-
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Whole-genome array comparative genome hybridization: The preferred diagnostics choice in postnatal clinical cytogenetics [1]
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Author keywords
[No Author keywords available]
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Indexed keywords
DNA;
CHROMOSOME ANALYSIS;
CHROMOSOME BANDING PATTERN;
COMPARATIVE GENOMIC HYBRIDIZATION;
CONGENITAL MALFORMATION;
CYTOGENETICS;
DATA ANALYSIS;
DIAGNOSTIC PROCEDURE;
DIAGNOSTIC VALUE;
DNA MICROARRAY;
GENETIC ANALYSIS;
GENETIC COUNSELING;
HUMAN;
INTERMETHOD COMPARISON;
LETTER;
MEDICAL DECISION MAKING;
MEDICAL RESEARCH;
MENTAL DEFICIENCY;
MICROARRAY ANALYSIS;
PATIENT CARE;
PERINATAL PERIOD;
TIME;
GENETIC SCREENING;
GENETICS;
GENOME;
NEWBORN;
NOTE;
NUCLEIC ACID HYBRIDIZATION;
POSTNATAL CARE;
CYTOGENETICS;
GENETIC SCREENING;
GENOME, HUMAN;
HUMANS;
INFANT, NEWBORN;
NUCLEIC ACID HYBRIDIZATION;
OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS;
POSTNATAL CARE;
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EID: 34247890199
PISSN: 15251578
EISSN: None
Source Type: Journal
DOI: 10.2353/jmoldx.2007.060187 Document Type: Letter |
Times cited : (14)
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References (5)
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