Monaco AP - Search Results

1

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. Nature. 1986 Oct 16-22;323(6089):646-50. doi: 10.1038/323646a0. Nature. 1986. PMID: 3773991

2

Isolation of a candidate gene for Norrie disease by positional cloning.

Berger W, Meindl A, van de Pol TJ, Cremers FP, Ropers HH, Döerner C, Monaco A, Bergen AA, Lebo R, Warburg M, et al. Berger W, et al. Nat Genet. 1992 Jun;1(3):199-203. doi: 10.1038/ng0692-199. Nat Genet. 1992. PMID: 1303235

3

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location.

Royer-Pokora B, Kunkel LM, Monaco AP, Goff SC, Newburger PE, Baehner RL, Cole FS, Curnutte JT, Orkin SH. Royer-Pokora B, et al. Among authors: monaco ap. Nature. 1986 Jul 3-9;322(6074):32-8. doi: 10.1038/322032a0. Nature. 1986. PMID: 2425263 Free article.

4

Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy.

Fischbeck KH, Ritter AW, Tirschwell DL, Kunkel LM, Bertelson CJ, Monaco AP, Hejtmancik JF, Boehm C, Ionasescu V, Ionasescu R, et al. Fischbeck KH, et al. Among authors: monaco ap. Lancet. 1986 Jul 12;2(8498):104. doi: 10.1016/s0140-6736(86)91634-x. Lancet. 1986. PMID: 2873362 Free article. No abstract available.

5

A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome.

van Ommen GJ, Verkerk JM, Hofker MH, Monaco AP, Kunkel LM, Ray P, Worton R, Wieringa B, Bakker E, Pearson PL. van Ommen GJ, et al. Among authors: monaco ap. Cell. 1986 Nov 21;47(4):499-504. doi: 10.1016/0092-8674(86)90614-8. Cell. 1986. PMID: 2877741

6

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: monaco ap. 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.

7

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

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

8

Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosome.

Chamberlain JS, Grant SG, Reeves AA, Mullins LJ, Stephenson DA, Hoffman EP, Monaco AP, Kunkel LM, Caskey CT, Chapman VM. Chamberlain JS, et al. Among authors: monaco ap. Somat Cell Mol Genet. 1987 Nov;13(6):671-8. doi: 10.1007/BF01534487. Somat Cell Mol Genet. 1987. PMID: 2890215

9

Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci.

Kunkel LM, Lalande M, Monaco AP, Flint A, Middlesworth W, Latt SA. Kunkel LM, et al. Among authors: monaco ap. Gene. 1985;33(3):251-8. doi: 10.1016/0378-1119(85)90232-x. Gene. 1985. PMID: 2989089

10

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.

Kunkel LM, Monaco AP, Middlesworth W, Ochs HD, Latt SA. Kunkel LM, et al. Among authors: monaco ap. Proc Natl Acad Sci U S A. 1985 Jul;82(14):4778-82. doi: 10.1073/pnas.82.14.4778. Proc Natl Acad Sci U S A. 1985. PMID: 2991893 Free PMC article.

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