Xie YG - Search Results

1

Restriction map of a YAC and cosmid contig encompassing the oculopharyngeal muscular dystrophy candidate region on chromosome 14q11.2-q13.

Xie YG, Rochefort D, Brais B, Howard H, Han FY, Gou LP, Maciel P, The BT, Larsson C, Rouleau GA. Xie YG, et al. Genomics. 1998 Sep 1;52(2):201-4. doi: 10.1006/geno.1998.5421. Genomics. 1998. PMID: 9782086

2

Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene.

Brais B, Bouchard JP, Gosselin F, Xie YG, Fardeau M, Tomé FM, Rouleau GA. Brais B, et al. Among authors: xie yg. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S70-4. doi: 10.1016/s0960-8966(97)00086-2. Neuromuscul Disord. 1997. PMID: 9392020

3

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.

Brais B, Bouchard JP, Xie YG, Rochefort DL, Chrétien N, Tomé FM, Lafrenière RG, Rommens JM, Uyama E, Nohira O, Blumen S, Korczyn AD, Heutink P, Mathieu J, Duranceau A, Codère F, Fardeau M, Rouleau GA. Brais B, et al. Among authors: xie yg. Nat Genet. 1998 Feb;18(2):164-7. doi: 10.1038/ng0298-164. Nat Genet. 1998. PMID: 9462747

4

Physical mapping of the NF2/meningioma region on human chromosome 22q12.

Ruttledge MH, Xie YG, Han FY, Giovannini M, Janson M, Fransson I, Werelius B, Delattre O, Thomas G, Evans G, et al. Ruttledge MH, et al. Among authors: xie yg. Genomics. 1994 Jan 1;19(1):52-9. doi: 10.1006/geno.1994.1012. Genomics. 1994. PMID: 8188242

5

The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13.

Brais B, Xie YG, Sanson M, Morgan K, Weissenbach J, Korczyn AD, Blumen SC, Fardeau M, Tomé FM, Bouchard JP, et al. Brais B, et al. Among authors: xie yg. Hum Mol Genet. 1995 Mar;4(3):429-34. doi: 10.1093/hmg/4.3.429. Hum Mol Genet. 1995. PMID: 7795598

6

Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12.

Xie YG, Han FY, Peyrard M, Ruttledge MH, Fransson I, DeJong P, Collins J, Dunham I, Nordenskjöld M, Dumanski JP. Xie YG, et al. Hum Mol Genet. 1993 Sep;2(9):1361-8. doi: 10.1093/hmg/2.9.1361. Hum Mol Genet. 1993. PMID: 8242058

7

Deletions on chromosome 22 in sporadic meningioma.

Ruttledge MH, Xie YG, Han FY, Peyrard M, Collins VP, Nordenskjöld M, Dumanski JP. Ruttledge MH, et al. Among authors: xie yg. Genes Chromosomes Cancer. 1994 Jun;10(2):122-30. doi: 10.1002/gcc.2870100207. Genes Chromosomes Cancer. 1994. PMID: 7520265

8

Identification, characterisation and clinical applications of cosmids from the telomeric and centromeric regions of the long arm of chromosome 22.

Xie YG, Han FY, Bajalica S, Blennow E, Kristoffersson U, Dumanski JP, Nordenskjöld M. Xie YG, et al. Hum Genet. 1994 Oct;94(4):339-45. doi: 10.1007/BF00201589. Hum Genet. 1994. PMID: 7927325

9

Direct and inverted reciprocal chromosome insertions between chromosomes 7 and 14 in a woman with recurrent miscarriages.

Wang YT, Bajalica S, Han FY, Wang ZC, Bui TH, Xie YG. Wang YT, et al. Among authors: xie yg. Am J Med Genet. 1994 Sep 1;52(3):349-51. doi: 10.1002/ajmg.1320520319. Am J Med Genet. 1994. PMID: 7810568

10

The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family.

Peyrard M, Seroussi E, Sandberg-Nordqvist AC, Xie YG, Han FY, Fransson I, Collins J, Dunham I, Kost-Alimova M, Imreh S, Dumanski JP. Peyrard M, et al. Among authors: xie yg. Proc Natl Acad Sci U S A. 1999 Jan 19;96(2):598-603. doi: 10.1073/pnas.96.2.598. Proc Natl Acad Sci U S A. 1999. PMID: 9892679 Free PMC article.

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