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My research interest, in the field of Duchenne muscular dystrophy (DMD), began ∼18 years ago. At the time, the DMD gene had not been identified, and our primary diagnostic tools were restriction fragment length polymorphism probes and creatine kinase measurements. This book is a tribute to the great progress that has been made since that time. Several of the authors have been major players in making it all possible. It is remarkable to observe how many of the scientific discoveries have had immediate impact on molecular testing and thus have benefited many families through more accurate diagnoses and counseling. …

clinical chemistry

Muscular Dystrophy: Methods and Protocols. Katherine M.D. Bushby and Louise V.B. Anderson, eds. Totowa, NJ: Humana Press, 2001, 436 pp., $99.50, hardcover. ISBN 0-89603-695-2.