Whole genome amplification from single cells in preimplantation genetic diagnosis and prenatal diagnosis

European Journal of Obstetrics and Gynecology and Reproductive Biology

Volumn 131, Issue 1, 2007, Pages 13-20

  Peng, Wen ^a,b   Takabayashi, Haruo ^b   Ikawa, Kazumi ^c  

^a SHANDONG PROVINCIAL HOSPITAL AFFILIATED TO SHANDONG UNIVERSITY   (China)

^b KANAZAWA MEDICAL UNIVERSITY   (Japan)

^c Ishikawa Health Service Association   (Japan)

Author keywords

Preimplantation genetic diagnosis; Prenatal diagnosis; Single cells; Whole genome amplification

Indexed keywords

OLIGONUCLEOTIDE;

ALLELE; BLASTOMERE; CHROMOSOME ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; DIAGNOSTIC ERROR; DIAGNOSTIC PROCEDURE; DNA CONTENT; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; HUMAN; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; REVIEW; SYSTEMATIC REVIEW;

EID: 33847153470     PISSN: 03012115     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejogrb.2006.07.027     Document Type: Review

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