Monaco AP - Search Results

1

A combination of the effects of rare genotypes at the XK and KEL blood group loci results in absence of Kell system antigens from the red blood cells.

Daniels GL, Weinauer F, Stone C, Ho M, Green CA, Jahn-Jochem H, Offner R, Monaco AP. Daniels GL, et al. Among authors: monaco ap. Blood. 1996 Nov 15;88(10):4045-50. Blood. 1996. PMID: 8916972 Free article.

2

Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.

Ho MF, Monaco AP, Blonden LA, van Ommen GJ, Affara NA, Ferguson-Smith MA, Lehrach H. Ho MF, et al. Among authors: monaco ap. Am J Hum Genet. 1992 Feb;50(2):317-30. Am J Hum Genet. 1992. PMID: 1734714 Free PMC article.

3

Isolation of CA dinucleotide repeats close to D6S105; linkage disequilibrium with haemochromatosis.

Stone C, Pointon JJ, Jazwinska EC, Halliday JW, Powell LW, Robson KJ, Monaco AP, Weatherall DJ. Stone C, et al. Among authors: monaco ap. Hum Mol Genet. 1994 Nov;3(11):2043-6. Hum Mol Genet. 1994. PMID: 7874124

4

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.

Ho M, Chelly J, Carter N, Danek A, Crocker P, Monaco AP. Ho M, et al. Among authors: monaco ap. Cell. 1994 Jun 17;77(6):869-80. doi: 10.1016/0092-8674(94)90136-8. Cell. 1994. PMID: 8004674

5

A novel point mutation in the McLeod syndrome gene in neuroacanthocytosis.

Ho MF, Chalmers RM, Davis MB, Harding AE, Monaco AP. Ho MF, et al. Among authors: monaco ap. Ann Neurol. 1996 May;39(5):672-5. doi: 10.1002/ana.410390518. Ann Neurol. 1996. PMID: 8619554

6

McLeod neuroacanthocytosis: genotype and phenotype.

Danek A, Rubio JP, Rampoldi L, Ho M, Dobson-Stone C, Tison F, Symmans WA, Oechsner M, Kalckreuth W, Watt JM, Corbett AJ, Hamdalla HH, Marshall AG, Sutton I, Dotti MT, Malandrini A, Walker RH, Daniels G, Monaco AP. Danek A, et al. Among authors: monaco ap. Ann Neurol. 2001 Dec;50(6):755-64. doi: 10.1002/ana.10035. Ann Neurol. 2001. PMID: 11761473

7

High-resolution comparative mapping of the proximal region of the mouse X chromosome.

Blair HJ, Ho M, Monaco AP, Fisher S, Craig IW, Boyd Y. Blair HJ, et al. Among authors: monaco ap. Genomics. 1995 Jul 20;28(2):305-10. doi: 10.1006/geno.1995.1146. Genomics. 1995. PMID: 8530041

8

Chorea-acanthocytosis: genetic linkage to chromosome 9q21.

Rubio JP, Danek A, Stone C, Chalmers R, Wood N, Verellen C, Ferrer X, Malandrini A, Fabrizi GM, Manfredi M, Vance J, Pericak-Vance M, Brown R, Rudolf G, Picard F, Alonso E, Brin M, Németh AH, Farrall M, Monaco AP. Rubio JP, et al. Among authors: monaco ap. Am J Hum Genet. 1997 Oct;61(4):899-908. doi: 10.1086/514876. Am J Hum Genet. 1997. PMID: 9382101 Free PMC article.

9

Chorein detection for the diagnosis of chorea-acanthocytosis.

Dobson-Stone C, Velayos-Baeza A, Filippone LA, Westbury S, Storch A, Erdmann T, Wroe SJ, Leenders KL, Lang AE, Dotti MT, Federico A, Mohiddin SA, Fananapazir L, Daniels G, Danek A, Monaco AP. Dobson-Stone C, et al. Among authors: monaco ap. Ann Neurol. 2004 Aug;56(2):299-302. doi: 10.1002/ana.20200. Ann Neurol. 2004. PMID: 15293285

10

Mutations and phenotype in isolated glycerol kinase deficiency.

Walker AP, Muscatelli F, Stafford AN, Chelly J, Dahl N, Blomquist HK, Delanghe J, Willems PJ, Steinmann B, Monaco AP. Walker AP, et al. Among authors: monaco ap. Am J Hum Genet. 1996 Jun;58(6):1205-11. Am J Hum Genet. 1996. PMID: 8651297 Free PMC article.

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