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Aldridge J, et al. A strategy to reveal high-frequency RFLPs along the human X chromosome. Am. J. Hum. Genet. 36: 546-564, 1984. PubMed: 6328976

Stambolian D, et al. Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis. Am. J. Hum. Genet. 47: 13-19, 1990. PubMed: 1971992

Pillers DA, et al. Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy. Am. J. Hum. Genet. 47: 795-801, 1990. PubMed: 2220819

Monaco AP, et al. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy. Hum. Genet. 75: 221-227, 1987. PubMed: 2881877

Louis M Kunkel, personal communication