Journal Article

Restriction fragment length polymorphisms on the short arm of X chromosome among the Japanese population

Michie Shimmoto, Akihiko Tsuji and Yoshiyuki Suzuki

Journal of Human Genetics, 1988, Volume 33, Number 3, Pages 333-338

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Journal Article

Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study

Anthonie J. Essen, Stephen Abbs, Montserrat Baiget, Egbert Bakker and Catherine Boileau, et al.

Human Genetics, 1991, Volume 88, Number 3, Pages 249-257

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Journal Article

DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases

J. C. Defesche, M. Visser, E. Bakker, G. Bouwsma and J. J. M. Vijlder, et al.

Human Genetics, 1989, Volume 82, Number 1, Pages 55-58

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Journal Article

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

Tsuneyuki Ubagai and Susumu Katayama

Journal of Human Genetics, 1991, Volume 36, Number 3, Pages 211-227

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Journal Article

Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus

T. Ried, V. Mahler, P. Vogt, L. Blonden and G. J. B. Ommen, et al.

Human Genetics, 1990, Volume 85, Number 6, Pages 581-586

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Journal Article

Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction

Satoshi Fujishita, Noritoshi Shibuya, Norio Niikawa and Shigenobu Nagataki

Journal of Human Genetics, 1991, Volume 36, Number 4, Pages 317-324

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Journal Article

Prenatal diagnosis of Duchenne muscular dystrophy: A three-year experience in a rapidly evolving field

E. Bakker, E. J. Bonten, H. Veenema, J. T. den Dunnen and P. M. Grootscholten, et al.

Journal of Inherited Metabolic Disease, 1989, Volume 12, Supplement 1, Pages 174-190

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Journal Article

A small deletion in the Duchenne/Becker muscular dystrophy locus —a functionally important region?

K. A. Hart, A. P. Monaco, L. M. Kunkel and M. Bobrow

Human Genetics, 1987, Volume 77, Number 1, Pages 88-91

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Journal Article

Diagnosis of genetic disease using recombinant DNA. Supplement

David N. Cooper and Jörg Schmidtke

Human Genetics, 1987, Volume 77, Number 1, Pages 66-75

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