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Gene diagnosis of duchenne muscular dystrophy and becker muscular dystrophy cdna and genomic clone probes


Gene diagnosis of duchenne muscular dystrophy and becker muscular dystrophy cdna and genomic clone probes



American Journal of Human Genetics 49(4 Suppl): 208



ISSN/ISBN: 0002-9297


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(PDF emailed within 1 workday: $29.90)

Accession: 031546949

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Related references

Usefulness of test: manual muscle testing, goniometry, and daily activities for differential diagnosis of Duchenne muscular dystrophy, Becker's mild muscular dystrophy and Becker's severe muscular dystrophy. International Journal of Rehabilitation Research. Internationale Zeitschrift für Rehabilitationsforschung. Revue Internationale de Recherches de Readaptation 21(1): 79-85, 1998

DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population. Jinrui Idengaku Zasshi. Japanese Journal of Human Genetics 36(3): 211-227, 1991

A cDNA clone from the Duchenne/Becker muscular dystrophy gene. Nature 328(6129): 434-437, 1987

Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patients. Journal of Cachexia Sarcopenia and Muscle 11(2): 547-563, 2020

Screening for deletions in duchenne and becker muscular dystrophy patients using the genomic probe p20 and the cdna xj10 1 2b 7b 8 and 44 1 8 probes. Revista Brasileira de Genetica 15(2): 469-481, 1992

Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes. Journal of Medical Genetics 26(1): 1-5, 1989

Genetic analysis of 60 Duchenne muscular dystrophy (DMD) or Becker muscular dystrophy (BMD) patients using dystrophin cDNA. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae 15(6): 399-404, 1993

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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. American Journal of Human Genetics 43(5): 620-629, 1988

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Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes. Journal of Medical Genetics 27(5): 292-297, 1990

Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy. American Journal of Medical Genetics 42(3): 281-287, 1992