Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays

Prenatal Diagnosis

Volumn 32, Issue 1, 2012, Pages 10-20

  Bi, Weimin ^a   Breman, Amy ^a   Shaw, Chad A ^a   Stankiewicz, Pawel ^a   Gambin, Tomasz ^a,b   Lu, Xinyan ^a   Cheung, Sau Wai ^a   Jackson, Laird G ^c   Lupski, James R ^a   den Veyver, Ignatia B Van ^a   Beaudet, Arthur L ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b WARSAW UNIVERSITY OF TECHNOLOGY   (Poland)

^c DREXEL UNIVERSITY COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

OLIGONUCLEOTIDE;

ANEUPLOIDY; ARTICLE; CHROMOSOME ABERRATION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; DIGEORGE SYNDROME; DNA MICROARRAY; FEMALE; FETUS CELL; GENE AMPLIFICATION; GENE DELETION; GENE DUPLICATION; GENOME; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL LINE; MALE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SINGLE CELL ANALYSIS; TRISOMY 21; WILLIAMS BEUREN SYNDROME;

ANEUPLOIDY; CELL LINE; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME DISORDERS; COMPARATIVE GENOMIC HYBRIDIZATION; DOWN SYNDROME; GENE DOSAGE; HUMANS; LYMPHOCYTES; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; OLIGONUCLEOTIDE PROBES; PREIMPLANTATION DIAGNOSIS; SINGLE-CELL ANALYSIS; WILLIAMS SYNDROME;

EID: 84857506553     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2855     Document Type: Article

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