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Year | Number of Results |
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1985 | 2 |
1986 | 3 |
1988 | 1 |
1989 | 1 |
2024 | 0 |
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Page 1
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Nature. 1986 Jul 3-9;322(6074):73-7. doi: 10.1038/322073a0.
Nature. 1986.
PMID: 3014348
Human X chromosome markers and Duchenne muscular dystrophy.
Davies KE, Speer A, Herrmann F, Spiegler AW, McGlade S, Hofker MH, Briand P, Hanke R, Schwartz M, Steinbicker V, et al.
Davies KE, et al. Among authors: mcglade s.
Nucleic Acids Res. 1985 May 24;13(10):3419-26. doi: 10.1093/nar/13.10.3419.
Nucleic Acids Res. 1985.
PMID: 3859837
Free PMC article.
Item in Clipboard
Tissue-specific regulation of avian vitamin D-dependent calcium-binding protein 28-kDa mRNA by 1,25-dihydroxyvitamin D3.
Clemens TL, McGlade SA, Garrett KP, Horiuchi N, Hendy GN.
Clemens TL, et al. Among authors: mcglade sa.
J Biol Chem. 1988 Sep 15;263(26):13112-6.
J Biol Chem. 1988.
PMID: 3417652
Free article.
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Molecular analysis of human X-linked diseases.
Davies KE, Ball SP, Dorkins HR, Forrest SM, Kenwrick SJ, King AW, Lavenir IJ, McGlade SA, Patterson MN, Smith TJ, et al.
Davies KE, et al. Among authors: mcglade sa.
Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:337-43. doi: 10.1101/sqb.1986.051.01.039.
Cold Spring Harb Symp Quant Biol. 1986.
PMID: 3472730
No abstract available.
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Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).
Davies KE, Mattei MG, Mattei JF, Veenema H, McGlade S, Harper K, Tommerup N, Nielsen KB, Mikkelsen M, Beighton P, et al.
Davies KE, et al. Among authors: mcglade s.
Hum Genet. 1985;70(3):249-55. doi: 10.1007/BF00273451.
Hum Genet. 1985.
PMID: 2991115
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Extracellular calcium modulates vitamin D-dependent calbindin-D28K gene expression in chick kidney cells.
Clemens TL, McGlade SA, Garrett KP, Craviso GL, Hendy GN.
Clemens TL, et al. Among authors: mcglade sa.
Endocrinology. 1989 Mar;124(3):1582-4. doi: 10.1210/endo-124-3-1582.
Endocrinology. 1989.
PMID: 2917526
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Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes.
Speer A, Davies K, McGlade S, Hanke R, Spiegler AW, Szibor R, Sommer D, Herrmann F, Coutelle C.
Speer A, et al. Among authors: mcglade s.
Biomed Biochim Acta. 1986;45(7):K19-27.
Biomed Biochim Acta. 1986.
PMID: 2878658
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