Speer MC - Search Results

1

Segregation analysis in cutaneous malignant melanoma/dysplastic nevus syndrome families.

Speer MC, Haynes CS, Pericak-Vance MA. Speer MC, et al. Cytogenet Cell Genet. 1992;59(2-3):225-7. doi: 10.1159/000133254. Cytogenet Cell Genet. 1992. PMID: 1737509 No abstract available.

2

Linkage studies in familial Alzheimer's disease.

Roses AD, Pericak-Vance MA, Yamaoka L, Haynes C, Speer M, Gaskell P, Hung WY, Clark CM, Heyman A, Trofatter J, et al. Roses AD, et al. Prog Clin Biol Res. 1989;317:201-15. Prog Clin Biol Res. 1989. PMID: 2602416 No abstract available.

3

Linkage analysis in familial amyotrophic lateral sclerosis.

Siddique T, Pericak-Vance MA, Brooks BR, Roos RP, Hung WY, Antel JP, Munsat TL, Phillips K, Warner K, Speer M, et al. Siddique T, et al. Neurology. 1989 Jul;39(7):919-25. doi: 10.1212/wnl.39.7.919. Neurology. 1989. PMID: 2739919

4

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

Johnson DW, Berg JN, Baldwin MA, Gallione CJ, Marondel I, Yoon SJ, Stenzel TT, Speer M, Pericak-Vance MA, Diamond A, Guttmacher AE, Jackson CE, Attisano L, Kucherlapati R, Porteous ME, Marchuk DA. Johnson DW, et al. Nat Genet. 1996 Jun;13(2):189-95. doi: 10.1038/ng0696-189. Nat Genet. 1996. PMID: 8640225

5

Multilocus mapping of the X-linked hypophosphatemic rickets gene.

Econs MJ, Barker DF, Speer MC, Pericak-Vance MA, Fain PR, Drezner MK. Econs MJ, et al. Among authors: speer mc. J Clin Endocrinol Metab. 1992 Jul;75(1):201-6. doi: 10.1210/jcem.75.1.1352307. J Clin Endocrinol Metab. 1992. PMID: 1352307

6

Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter.

Speer MC, Goldgaber D, Goldfarb LG, Roses AD, Pericak-Vance MA. Speer MC, et al. Genomics. 1991 Feb;9(2):366-8. doi: 10.1016/0888-7543(91)90266-h. Genomics. 1991. PMID: 1672296

7

The human glycine receptor: a new probe that is linked to the X-linked hypophosphatemic rickets gene.

Econs MJ, Pericak-Vance MA, Betz H, Bartlett RJ, Speer MC, Drezner MK. Econs MJ, et al. Among authors: speer mc. Genomics. 1990 Jul;7(3):439-41. doi: 10.1016/0888-7543(90)90180-3. Genomics. 1990. PMID: 2163973

8

Linkage studies of late-onset familial Alzheimer's disease.

Roses AD, Pericak-Vance MA, Clark CM, Gilbert JR, Yamaoka LH, Haynes CS, Speer MC, Gaskell PC, Hung WY, Trofatter JA, et al. Roses AD, et al. Among authors: speer mc. Adv Neurol. 1990;51:185-96. Adv Neurol. 1990. PMID: 2294655 No abstract available.

9

Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19.

Yamaoka LH, Pericak-Vance MA, Speer MC, Gaskell PC Jr, Stajich J, Haynes C, Hung WY, Laberge C, Thibault MC, Mathieu J, et al. Yamaoka LH, et al. Among authors: speer mc. Neurology. 1990 Feb;40(2):222-6. doi: 10.1212/wnl.40.2.222. Neurology. 1990. PMID: 2300239

10

Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studies.

Speer MC, Pericak-Vance MA, Yamaoka L, Hung WY, Ashley A, Stajich JM, Roses AD. Speer MC, et al. Neurology. 1990 Apr;40(4):671-6. doi: 10.1212/wnl.40.4.671. Neurology. 1990. PMID: 2320244

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