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Volumn 31, Issue 4, 2011, Pages 581-594

Clinical utility of single nucleotide polymorphism arrays

Author keywords

Consanguinity; Oncology arrays; Prenatal arrays; Runs of homozygosity; Single nucleotide polymorphism microarray; Uniparental disomy

Indexed keywords

BACTERIAL ARTIFICIAL CHROMOSOME; CHROMOSOME ANALYSIS; CHRONIC LYMPHATIC LEUKEMIA; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; CYTOGENETICS; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DOSAGE; GENE DUPLICATION; GENE FREQUENCY; GENOTYPE; HETEROZYGOSITY; HETEROZYGOSITY LOSS; HOMOZYGOSITY; HUMAN; LIMB GIRDLE MUSCULAR DYSTROPHY; MICROARRAY ANALYSIS; MISSENSE MUTATION; MOSAICISM; OLIGONUCLEOTIDE PROBE; PRIORITY JOURNAL; REVIEW; RNA PROBE; SINGLE NUCLEOTIDE POLYMORPHISM; UNIPARENTAL DISOMY;

EID: 82355184558     PISSN: 02722712     EISSN: 15579832     Source Type: Journal    
DOI: 10.1016/j.cll.2011.09.002     Document Type: Review
Times cited : (18)

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