Spence MA - Search Results

1

Mapping studies of the serum cholinesterase-2 locus (CHE2).

Marazita ML, Keats BJ, Spence MA, Sparkes RS, Field LL, Sparkes MC, Crist M. Marazita ML, et al. Among authors: spence ma. Hum Genet. 1989 Sep;83(2):139-44. doi: 10.1007/BF00286706. Hum Genet. 1989. PMID: 2777253

2

Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.

Kojis TL, Heinzmann C, Flodman P, Ngo JT, Sparkes RS, Spence MA, Bateman JB, Heckenlively JR. Kojis TL, et al. Among authors: spence ma. Am J Hum Genet. 1996 Feb;58(2):347-55. Am J Hum Genet. 1996. PMID: 8571961 Free PMC article.

3

Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1.

Spence MA, Sparkes RS, Heckenlively JR, Pearlman JT, Zedalis D, Sparkes M, Crist M, Tideman S. Spence MA, et al. Am J Hum Genet. 1977 Jul;29(4):397-404. Am J Hum Genet. 1977. PMID: 879170 Free PMC article.

4

Cleft lip with or without cleft palate in Shanghai, China: evidence for an autosomal major locus.

Marazita ML, Hu DN, Spence MA, Liu YE, Melnick M. Marazita ML, et al. Among authors: spence ma. Am J Hum Genet. 1992 Sep;51(3):648-53. Am J Hum Genet. 1992. PMID: 1307687 Free PMC article.

5

Genetic linkage studies with neurofibromatosis: the question of heterogeneity.

Spence MA, Sparkes RS, Parry DM, Bale SJ, Cortessis V, Mulvihill JJ. Spence MA, et al. J Med Genet. 1987 Sep;24(9):527-9. doi: 10.1136/jmg.24.9.527. J Med Genet. 1987. PMID: 3118031 Free PMC article.

6

Genetic linkage analysis of autosomal dominant congenital cataracts.

Bateman JB, Spence MA, Marazita ML, Sparkes RS. Bateman JB, et al. Among authors: spence ma. Am J Ophthalmol. 1986 Feb 15;101(2):218-25. doi: 10.1016/0002-9394(86)90599-4. Am J Ophthalmol. 1986. PMID: 3456204

7

Gene mapping studies with the syndrome of autism.

Spence MA, Ritvo ER, Marazita ML, Funderburk SJ, Sparkes RS, Freeman BJ. Spence MA, et al. Behav Genet. 1985 Jan;15(1):1-13. doi: 10.1007/BF01071928. Behav Genet. 1985. PMID: 3985910 No abstract available.

8

Genetic linkage analysis of the carpal tunnel syndrome.

Sparkes RS, Spence MA, Gottlieb NL, Gray RG, Crist M, Sparkes MC, Marazita M. Sparkes RS, et al. Among authors: spence ma. Hum Hered. 1985;35(5):288-91. doi: 10.1159/000153564. Hum Hered. 1985. PMID: 4043979

9

Linkage analysis of neurofibromatosis (von Recklinghausen disease).

Spence MA, Bader JL, Parry DM, Field LL, Funderburk SJ, Rubenstein AE, Gilman PA, Sparkes RS. Spence MA, et al. J Med Genet. 1983 Oct;20(5):334-7. doi: 10.1136/jmg.20.5.334. J Med Genet. 1983. PMID: 6417334 Free PMC article.

10

Estimating the recombination frequency for the MN and the Ss loci.

Spence MA, Field LL, Marazita ML, Joseph J, Sparkes M, Crist M, Crandall BF, Anderson CE, Bateman JB, Rotter JI, et al. Spence MA, et al. Hum Hered. 1984;34(6):343-7. doi: 10.1159/000153494. Hum Hered. 1984. PMID: 6510930

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