Colletti-Feener C - Search Results

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Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.

Monaco AP, Neve RL, Colletti-Feener C, Bertelson CJ, Kurnit DM, Kunkel LM. Monaco AP, et al. Among authors: colletti feener c. Nature. 1986 Oct 16-22;323(6089):646-50. doi: 10.1038/323646a0. Nature. 1986. PMID: 3773991

Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.

Bertelson CJ, Bartley JA, Monaco AP, Colletti-Feener C, Fischbeck K, Kunkel LM. Bertelson CJ, et al. Among authors: colletti feener c. J Med Genet. 1986 Dec;23(6):531-7. doi: 10.1136/jmg.23.6.531. J Med Genet. 1986. PMID: 2879924 Free PMC article.

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.

Monaco AP, Bertelson CJ, Colletti-Feener C, Kunkel LM. Monaco AP, et al. Among authors: colletti feener c. Hum Genet. 1987 Mar;75(3):221-7. doi: 10.1007/BF00281063. Hum Genet. 1987. PMID: 2881877

Rapid cloning of multiple amplified nucleotide sequences from human neuroblastoma cell lines by phenol emulsion competitive DNA reassociation.

Shiloh Y, Rose E, Colletti-Feener C, Korf B, Kunkel LM, Latt SA. Shiloh Y, et al. Among authors: colletti feener c. Gene. 1987;51(1):53-9. doi: 10.1016/0378-1119(87)90473-2. Gene. 1987. PMID: 3596238

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