Wagner M - Search Results

1

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.

Lopes-Cendes I, Andermann E, Attig E, Cendes F, Bosch S, Wagner M, Gerstenbrand F, Andermann F, Rouleau GA. Lopes-Cendes I, et al. Among authors: wagner m. Am J Hum Genet. 1994 May;54(5):774-81. Am J Hum Genet. 1994. PMID: 8178818 Free PMC article.

2

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.

3

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

4

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

5

Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis.

Ni L, Wagner MJ, Kimberling WJ, Pembrey ME, Grundfast KM, Kumar S, Daiger SP, Wells DE, Johnson K, Smith RJ. Ni L, et al. Among authors: wagner mj. Am J Med Genet. 1994 Jun 1;51(2):176-84. doi: 10.1002/ajmg.1320510222. Am J Med Genet. 1994. PMID: 8092199

6

Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome.

Lüdecke HJ, Johnson C, Wagner MJ, Wells DE, Turleau C, Tommerup N, Latos-Bielenska A, Sandig KR, Meinecke P, Zabel B, et al. Lüdecke HJ, et al. Among authors: wagner mj. Am J Hum Genet. 1991 Dec;49(6):1197-206. Am J Hum Genet. 1991. PMID: 1836105 Free PMC article.

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

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.

9

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.

10

Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndrome.

Lüdecke HJ, Wagner MJ, Nardmann J, La Pillo B, Parrish JE, Willems PJ, Haan EA, Frydman M, Hamers GJ, Wells DE, et al. Lüdecke HJ, et al. Among authors: wagner mj. Hum Mol Genet. 1995 Jan;4(1):31-6. doi: 10.1093/hmg/4.1.31. Hum Mol Genet. 1995. PMID: 7711731

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