Ranier JE - Search Results

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Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification.

Ballabio A, Ranier JE, Chamberlain JS, Zollo M, Caskey CT. Ballabio A, et al. Among authors: ranier je. Hum Genet. 1990 May;84(6):571-3. doi: 10.1007/BF00210812. Hum Genet. 1990. PMID: 2338343 Free article.

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification.

Chamberlain JS, Gibbs RA, Ranier JE, Nguyen PN, Caskey CT. Chamberlain JS, et al. Among authors: ranier je. Nucleic Acids Res. 1988 Dec 9;16(23):11141-56. doi: 10.1093/nar/16.23.11141. Nucleic Acids Res. 1988. PMID: 3205741 Free PMC article.

Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy.

Pillers DA, Towbin JA, Chamberlain JS, Wu D, Ranier J, Powell BR, McCabe ER. Pillers DA, et al. Am J Hum Genet. 1990 Nov;47(5):795-801. Am J Hum Genet. 1990. PMID: 2220819 Free PMC article.

Expression of the murine Duchenne muscular dystrophy gene in muscle and brain.

Chamberlain JS, Pearlman JA, Muzny DM, Gibbs RA, Ranier JE, Caskey CT, Reeves AA. Chamberlain JS, et al. Among authors: ranier je. Science. 1988 Mar 18;239(4846):1416-8. doi: 10.1126/science.3347839. Science. 1988. PMID: 3347839

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