Yu S - Search Results

1

Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins.

Richards RI, Holman K, Yu S, Sutherland GR. Richards RI, et al. Among authors: yu s. Hum Mol Genet. 1993 Sep;2(9):1429-35. doi: 10.1093/hmg/2.9.1429. Hum Mol Genet. 1993. PMID: 8242066

2

Fragile X syndrome without CCG amplification has an FMR1 deletion.

Gedeon AK, Baker E, Robinson H, Partington MW, Gross B, Manca A, Korn B, Poustka A, Yu S, Sutherland GR, et al. Gedeon AK, et al. Among authors: yu s. Nat Genet. 1992 Aug;1(5):341-4. doi: 10.1038/ng0892-341. Nat Genet. 1992. PMID: 1302032

3

Fragile-X syndrome: unique genetics of the heritable unstable element.

Yu S, Mulley J, Loesch D, Turner G, Donnelly A, Gedeon A, Hillen D, Kremer E, Lynch M, Pritchard M, et al. Yu S, et al. Am J Hum Genet. 1992 May;50(5):968-80. Am J Hum Genet. 1992. PMID: 1570846 Free PMC article.

4

Experience with direct molecular diagnosis of fragile X.

Mulley JC, Yu S, Gedeon AK, Donnelly A, Turner G, Loesch D, Chapman CJ, Gardner RJ, Richards RI, Sutherland GR. Mulley JC, et al. Among authors: yu s. J Med Genet. 1992 Jun;29(6):368-74. doi: 10.1136/jmg.29.6.368. J Med Genet. 1992. PMID: 1619631 Free PMC article.

5

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.

Kremer EJ, Pritchard M, Lynch M, Yu S, Holman K, Baker E, Warren ST, Schlessinger D, Sutherland GR, Richards RI. Kremer EJ, et al. Among authors: yu s. Science. 1991 Jun 21;252(5013):1711-4. doi: 10.1126/science.1675488. Science. 1991. PMID: 1675488

6

Hereditary unstable DNA: a new explanation for some old genetic questions?

Sutherland GR, Haan EA, Kremer E, Lynch M, Pritchard M, Yu S, Richards RI. Sutherland GR, et al. Among authors: yu s. Lancet. 1991 Aug 3;338(8762):289-92. doi: 10.1016/0140-6736(91)90426-p. Lancet. 1991. PMID: 1677119

7

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.

Richards RI, Holman K, Kozman H, Kremer E, Lynch M, Pritchard M, Yu S, Mulley J, Sutherland GR. Richards RI, et al. Among authors: yu s. J Med Genet. 1991 Dec;28(12):818-23. doi: 10.1136/jmg.28.12.818. J Med Genet. 1991. PMID: 1757956 Free PMC article.

8

Isolation of a human DNA sequence which spans the fragile X.

Kremer EJ, Yu S, Pritchard M, Nagaraja R, Heitz D, Lynch M, Baker E, Hyland VJ, Little RD, Wada M, et al. Kremer EJ, et al. Among authors: yu s. Am J Hum Genet. 1991 Sep;49(3):656-61. Am J Hum Genet. 1991. PMID: 1882843 Free PMC article.

9

Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence.

Sutherland GR, Gedeon A, Kornman L, Donnelly A, Byard RW, Mulley JC, Kremer E, Lynch M, Pritchard M, Yu S, et al. Sutherland GR, et al. Among authors: yu s. N Engl J Med. 1991 Dec 12;325(24):1720-2. doi: 10.1056/NEJM199112123252407. N Engl J Med. 1991. PMID: 1944473 Free article. No abstract available.

10

Fragile X genotype characterized by an unstable region of DNA.

Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D, et al. Yu S, et al. Science. 1991 May 24;252(5009):1179-81. doi: 10.1126/science.252.5009.1179. Science. 1991. PMID: 2031189

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