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

Author:

Zeng Fanyi,Ren Zhao-Rui,Huang Shang-Zhi,Kalf Margot,Mommersteeg Monique,Smit Maarten,White Stefan,Jin Chun-Lian,Xu Miao,Zhou Da-Wen,Yan Jing-Bin,Chen Mei-Jue,van Beuningen Rinie,Huang Shu-Zhen,den Dunnen Johan,Zeng Yi-Tao,Wu Ying

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods;Abbs;J Med Genet,1991

2. Measurement of locus copy number by hybridisation with amplifiable probes;Armour;Nucleic Acids Res,2000

3. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations;Darras;Am J Hum Genet,1988

4. Topography of the Duchenne muscular-dystrophy (DMD) gene-FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications;den Dunnen;Am J Hum Genet,1989

5. Population frequencies of inherited neuromuscular diseases-a world survey;Emery;Neuromuscul Disord,1991

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