Fluorescence in situ hybridization establishes the order cen-DXS28(C7)-DXS67(B24)-DXS68(L1)-tel in human chromosome Xp21.3

Author:

Trask Barbara J.,Massa Hillary F.,Burmeister Margit

Publisher

Elsevier BV

Subject

Genetics

Reference15 articles.

1. A Xp21 deletion assigns locus DXS28 (C7) proximal to DXS68 (L1.4) and DXS67 (B24) and has the proximal breakpoint in the intron 3′ to the first exon of DMD-8 (DMD exon 47);Bartley;Cytogenet. Cell Genet,1989

2. Long-range restriction map around the Duchenne muscular dystrophy gene;Burmeister;Nature,1986

3. A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene;Burmeister;Genomics,1988

4. Localization of DNA sequences in region Xp21 of the human X chromosome: Search for molecular markers close to the Duchenne muscular dystrophy locus;De Martinville;Am. J. Hum. Genet,1985

5. Lambda replacement vectors carrying polylinker sequences;Frischauf;J. Mol. Biol,1983

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