Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy

Molecular Cytogenetics

Volumn 7, Issue 1, 2014, Pages

  Bug, Stefanie ^a   Solfrank, Beate ^a   Schmitz, Felizitas ^a   Pricelius, Jana ^a   Stecher, Mona ^a   Craig, Andrew ^b   Botcherby, Marc ^b   Nevinny Stickel Hinzpeter, Claudia ^a  

^a Synlab Medizinisches Versorgungszentrum Humane Genetik München ^*  (Germany)

^b ILLUMINA INC   (United States)

Author keywords

Aneuploidy; Combined microarray; Early pregnancy loss; Genetic diagnostics; Loss of heterozygosity; Product of conception

Indexed keywords

GENOMIC DNA; OLIGONUCLEOTIDE;

ANEUPLOIDY; ARTICLE; CHROMOSOME 11; CHROMOSOME 21; CHROMOSOME ABERRATION; COHORT ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DIAGNOSTIC TEST ACCURACY STUDY; DIAGNOSTIC VALUE; DNA EXTRACTION; DNA HYBRIDIZATION; FETUS; FOLLOW UP; GENE DOSAGE; GENETIC ASSOCIATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; HYDATIDIFORM MOLE; KARYOTYPE; MICROARRAY ANALYSIS; MONOSOMY X; PREGNANCY OUTCOME; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TETRAPLOIDY; TRIPLOIDY; UNIPARENTAL DISOMY; X CHROMOSOME;

EID: 84904302424     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-7-43     Document Type: Article

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