Speer MC - Search Results

1

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C, et al. Hentati A, et al. Among authors: speer mc. Nat Genet. 1994 Jul;7(3):425-8. doi: 10.1038/ng0794-425. Nat Genet. 1994. PMID: 7920663

2

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

Messina DN, Speer MC, Pericak-Vance MA, McNally EM. Messina DN, et al. Among authors: speer mc. Am J Hum Genet. 1997 Oct;61(4):909-17. doi: 10.1086/514896. Am J Hum Genet. 1997. PMID: 9382102 Free PMC article.

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

Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!

Kandt RS, Pericak-Vance MA, Hung WY, Gardner RJ, Crossen PE, Nellist MD, Speer MC, Roses AD. Kandt RS, et al. Among authors: speer mc. Ann N Y Acad Sci. 1991;615:284-97. doi: 10.1111/j.1749-6632.1991.tb37770.x. Ann N Y Acad Sci. 1991. PMID: 2039152

5

Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I.

Vance JM, Pericak-Vance MA, Yamaoka LH, Speer MC, Rosenwasser GO, Small K, Gaskell PC Jr, Hung WY, Alberts MJ, Haynes CS, et al. Vance JM, et al. Among authors: speer mc. Am J Hum Genet. 1989 Jan;44(1):25-9. Am J Hum Genet. 1989. PMID: 2491777 Free PMC article.

6

Absence of linkage of ABO blood group locus to familial tuberous sclerosis.

Kandt RS, Pericak-Vance MA, Hung WY, Gardner RJ, Nellist M, Phillips K, Warner K, Speer MC, Crossen PE, Laing NG, et al. Kandt RS, et al. Among authors: speer mc. Exp Neurol. 1989 Jun;104(3):223-8. doi: 10.1016/0014-4886(89)90033-2. Exp Neurol. 1989. PMID: 2721625

7

Familial inheritance of a DXS164 deletion mutation from a heterozygous female.

Lanman JT Jr, Pericak-Vance MA, Bartlett RJ, Chen JC, Yamaoka L, Koh J, Speer MC, Hung WY, Roses AD. Lanman JT Jr, et al. Among authors: speer mc. Am J Hum Genet. 1987 Aug;41(2):138-44. Am J Hum Genet. 1987. PMID: 2887110 Free PMC article.

8

Genetic linkage studies of chromosome 17 RFLPs in von Recklinghausen neurofibromatosis (NF1).

Pericak-Vance MA, Yamaoka LH, Vance JM, Small K, Rosenwasser GO, Gaskell PC Jr, Hung WY, Alberts MJ, Haynes CS, Speer MC, et al. Pericak-Vance MA, et al. Among authors: speer mc. Genomics. 1987 Dec;1(4):349-52. doi: 10.1016/0888-7543(87)90036-x. Genomics. 1987. PMID: 3130305

9

Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37.

Speer MC, Tandan R, Rao PN, Fries T, Stajich JM, Bolhuis PA, Jöbsis GJ, Vance JM, Viles KD, Sheffield K, James C, Kahler SG, Pettenati M, Gilbert JR, Denton PH, Yamaoka LH, Pericak-Vance MA. Speer MC, et al. Hum Mol Genet. 1996 Jul;5(7):1043-6. doi: 10.1093/hmg/5.7.1043. Hum Mol Genet. 1996. PMID: 8817344

10

Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31.

Bartoloni L, Horrigan SK, Viles KD, Gilchrist JM, Stajich JM, Vance JM, Yamaoka LH, Pericak-Vance MA, Westbrook CA, Speer MC. Bartoloni L, et al. Among authors: speer mc. Genomics. 1998 Dec 1;54(2):250-5. doi: 10.1006/geno.1998.5579. Genomics. 1998. PMID: 9828127

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