Magenis RE - Search Results

1

Ordering of Y-specific sequences by deletion mapping and analysis of X-Y interchange males and females.

Ferguson-Smith MA, Affara NA, Magenis RE. Ferguson-Smith MA, et al. Among authors: magenis re. Development. 1987;101 Suppl:41-50. doi: 10.1242/dev.101.Supplement.41. Development. 1987. PMID: 3503721

2

Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes.

Affara NA, Ferguson-Smith MA, Magenis RE, Tolmie JL, Boyd E, Cooke A, Jamieson D, Kwok K, Mitchell M, Snadden L. Affara NA, et al. Among authors: magenis re. Nucleic Acids Res. 1987 Sep 25;15(18):7325-42. doi: 10.1093/nar/15.18.7325. Nucleic Acids Res. 1987. PMID: 3658694 Free PMC article.

3

Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)n.

Weber B, Collins C, Robbins C, Magenis RE, Delaney AD, Gray JW, Hayden MR. Weber B, et al. Among authors: magenis re. Nucleic Acids Res. 1990 Jun 11;18(11):3353-61. doi: 10.1093/nar/18.11.3353. Nucleic Acids Res. 1990. PMID: 2356126 Free PMC article.

4

Y-derived sequences detected in a 45,X male by in situ hybridization.

Sheehy RR, Brown MG, Warren RJ, Schwartzman M, Magenis RE. Sheehy RR, et al. Among authors: magenis re. Am J Med Genet. 1987 Aug;27(4):831-9. doi: 10.1002/ajmg.1320270411. Am J Med Genet. 1987. PMID: 3321991 Review.

5

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.

Knoll JH, Nicholls RD, Magenis RE, Graham JM Jr, Lalande M, Latt SA. Knoll JH, et al. Among authors: magenis re. Am J Med Genet. 1989 Feb;32(2):285-90. doi: 10.1002/ajmg.1320320235. Am J Med Genet. 1989. PMID: 2564739

6

Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe.

Magenis RE, Casanova M, Fellous M, Olson S, Sheehy R. Magenis RE, et al. Hum Genet. 1987 Mar;75(3):228-33. doi: 10.1007/BF00281064. Hum Genet. 1987. PMID: 3557449

7

Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.

Knoll JH, Nicholls RD, Magenis RE, Glatt K, Graham JM Jr, Kaplan L, Lalande M. Knoll JH, et al. Among authors: magenis re. Am J Hum Genet. 1990 Jul;47(1):149-54. Am J Hum Genet. 1990. PMID: 1971993 Free PMC article.

8

Parental origin of the extra chromosome in the cat eye syndrome: evidence from heteromorphism and in situ hybridization analysis.

Magenis RE, Sheehy RR, Brown MG, McDermid HE, White BN, Zonana J, Weleber R. Magenis RE, et al. Am J Med Genet. 1988 Jan;29(1):9-19. doi: 10.1002/ajmg.1320290103. Am J Med Genet. 1988. PMID: 3344779

9

Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).

Greenberg F, Guzzetta V, Montes de Oca-Luna R, Magenis RE, Smith AC, Richter SF, Kondo I, Dobyns WB, Patel PI, Lupski JR. Greenberg F, et al. Among authors: magenis re. Am J Hum Genet. 1991 Dec;49(6):1207-18. Am J Hum Genet. 1991. PMID: 1746552 Free PMC article.

10

Seven polymorphic loci mapping to human chromosomal region 11q22-qter.

Maslen CL, Jones C, Glaser T, Magenis RE, Sheehy R, Kellogg J, Litt M. Maslen CL, et al. Among authors: magenis re. Genomics. 1988 Jan;2(1):66-75. doi: 10.1016/0888-7543(88)90110-3. Genomics. 1988. PMID: 2898428

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