Wagner M - Search Results

1

Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies.

Hecht JT, Hogue D, Wang Y, Blanton SH, Wagner M, Strong LC, Raskind W, Hansen MF, Wells D. Hecht JT, et al. Among authors: wagner m. Am J Hum Genet. 1997 Jan;60(1):80-6. Am J Hum Genet. 1997. PMID: 8981950 Free PMC article.

2

Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11.

Blanton SH, Hogue D, Wagner M, Wells D, Young ID, Hecht JT. Blanton SH, et al. Among authors: wagner m. Am J Med Genet. 1996 Mar 15;62(2):150-9. doi: 10.1002/(SICI)1096-8628(19960315)62:2<150::AID-AJMG7>3.0.CO;2-#. Am J Med Genet. 1996. PMID: 8882395

3

Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8.

Hecht JT, Hogue D, Strong LC, Hansen MF, Blanton SH, Wagner M. Hecht JT, et al. Among authors: wagner m. Am J Hum Genet. 1995 May;56(5):1125-31. Am J Hum Genet. 1995. PMID: 7726168 Free PMC article.

4

Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1).

Ahn J, Lüdecke HJ, Lindow S, Horton WA, Lee B, Wagner MJ, Horsthemke B, Wells DE. Ahn J, et al. Among authors: wagner mj. Nat Genet. 1995 Oct;11(2):137-43. doi: 10.1038/ng1095-137. Nat Genet. 1995. PMID: 7550340

5

Tetranucleotide repeat polymorphism (D8S582) for human EST00680 (D8S340E).

Sullivan LS, Parrish J, Wagner MJ, Wells D, Blanton SH, Daiger SP. Sullivan LS, et al. Among authors: wagner mj. Hum Mol Genet. 1994 Feb;3(2):386. doi: 10.1093/hmg/3.2.386-a. Hum Mol Genet. 1994. PMID: 8004122 No abstract available.

6

Identification of novel mutations in the human EXT1 tumor suppressor gene.

Wells DE, Hill A, Lin X, Ahn J, Brown N, Wagner MJ. Wells DE, et al. Among authors: wagner mj. Hum Genet. 1997 May;99(5):612-5. doi: 10.1007/s004390050415. Hum Genet. 1997. PMID: 9150727

7

Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses.

Raskind WH, Conrad EU 3rd, Matsushita M, Wijsman EM, Wells DE, Chapman N, Sandell LJ, Wagner M, Houck J. Raskind WH, et al. Among authors: wagner m. Hum Mutat. 1998;11(3):231-9. doi: 10.1002/(SICI)1098-1004(1998)11:3<231::AID-HUMU8>3.0.CO;2-K. Hum Mutat. 1998. PMID: 9521425

8

Dinucleotide repeat polymorphism at the CRH gene.

Gu J, Sadler L, Daiger S, Wells D, Wagner M. Gu J, et al. Among authors: wagner m. Hum Mol Genet. 1993 Jan;2(1):85. doi: 10.1093/hmg/2.1.85. Hum Mol Genet. 1993. PMID: 8490628 No abstract available.

9

Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome.

Parrish JE, Wagner MJ, Hecht JT, Scott CI Jr, Wells DE. Parrish JE, et al. Among authors: wagner mj. Genomics. 1991 Sep;11(1):54-61. doi: 10.1016/0888-7543(91)90101-j. Genomics. 1991. PMID: 1684953

10

Alignment of physical and genetic maps of human 8q23-qter using somatic cell hybrid mapping panel.

Parrish JE, Wang Y, Wagner MJ, Wells DE. Parrish JE, et al. Among authors: wagner mj. Somat Cell Mol Genet. 1994 Mar;20(2):143-6. doi: 10.1007/BF02290684. Somat Cell Mol Genet. 1994. PMID: 8009368

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