1. Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and random inactivation of the normal X chromosome;Verellen-Dumoulin;Hu, Genet,1984
2. A cDNA clone from the Duchenne/Becker muscular dystrophy gene;Burghes;Nature,1987
3. Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinis pigmentosa, and McLeod Syndrome;Francke;Am J Hum Genet,1985
4. Specific cloning fragments absent from the DNA of a male patient with an X chromosome deletion;Kunkel,1985
5. Mendelian Inheritance in Man;McKusick,1992