Array-MLPA: Comprehensive detection of deletions and duplications and its application to DMD patients

Human Mutation

Volumn 29, Issue 1, 2008, Pages 190-197

  Zeng, Fanyi ^a   Ren, Zhao Rui ^a   Huang, Shang Zhi ^b   Kalf, Margot ^c   Mommersteeg, Monique ^d   Smit, Maarten ^d   White, Stefan ^c   Jin, Chun Lian ^e   Xu, Miao ^a   Zhou, Da Wen ^a   Yan, Jing Bin ^a   Chen, Mei Jue ^a   Van Beuningen, Rinie ^d   Huang, Shu Zhen ^a   Dunnen, Johan Den ^c   Zeng, Yi Tao ^a   Wu, Ying ^a,d  

^a SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

^b INSTITUTE OF BASIC MEDICAL SCIENCES   (China)

^c LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^d PamGene International BV   (Netherlands)

^e CHINA MEDICAL UNIVERSITY   (China)

Author keywords

DMD; Duchenne muscular dystrophy; Microarray; MLPA

Indexed keywords

ARRAY MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; ARTICLE; AUTOMATION; BASE PAIRING; CHINA; CHINESE; CONTROLLED STUDY; DATA ANALYSIS; DMD GENE; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; GENE; GENE DELETION; GENE DUPLICATION; GENE REARRANGEMENT; GENE SEQUENCE; GENETIC SCREENING; GENOTYPE; HIGH THROUGHPUT SCREENING; HUMAN; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SIGNAL DETECTION; VARIANCE;

FEMALE; GENE DELETION; GENE DUPLICATION; GENETIC SCREENING; HUMANS; MALE; MUSCULAR DYSTROPHY, DUCHENNE; NUCLEIC ACID AMPLIFICATION TECHNIQUES;

EID: 38149091561     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20613     Document Type: Article

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