Blanton SH - Search Results

1

Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyelocele.

Au KS, Northrup H, Kirkpatrick TJ, Volcik KA, Fletcher JM, Townsend IT, Blanton SH, Tyerman GH, Villarreal G, King TM. Au KS, et al. Among authors: blanton sh. Am J Med Genet A. 2005 Dec 15;139(3):194-8. doi: 10.1002/ajmg.a.31002. Am J Med Genet A. 2005. PMID: 16283668 Free PMC article.

2

Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics.

Volcik KA, Blanton SH, Tyerman GH, Jong ST, Rott EJ, Page TZ, Romaine NK, Northrup H. Volcik KA, et al. Among authors: blanton sh. Am J Med Genet. 2000 Nov 6;95(1):21-7. Am J Med Genet. 2000. PMID: 11074490

3

Testing for genetic associations with the PAX gene family in a spina bifida population.

Volcik KA, Blanton SH, Kruzel MC, Townsend IT, Tyerman GH, Mier RJ, Northrup H. Volcik KA, et al. Among authors: blanton sh. Am J Med Genet. 2002 Jul 1;110(3):195-202. doi: 10.1002/ajmg.10434. Am J Med Genet. 2002. PMID: 12116225

4

Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects.

Volcik KA, Blanton SH, Kruzel MC, Townsend IT, Tyerman GH, Mier RJ, Northrup H. Volcik KA, et al. Among authors: blanton sh. Am J Med Genet. 2002 Jul 1;110(3):203-7. doi: 10.1002/ajmg.10435. Am J Med Genet. 2002. PMID: 12116226

5

Apoptotic gene analysis in idiopathic talipes equinovarus (clubfoot).

Ester AR, Tyerman G, Wise CA, Blanton SH, Hecht JT. Ester AR, et al. Among authors: blanton sh. Clin Orthop Relat Res. 2007 Sep;462:32-7. doi: 10.1097/BLO.0b013e318073c2d9. Clin Orthop Relat Res. 2007. PMID: 17534194

6

Evaluation of candidate genes for familial brachydactyly.

Mastrobattista JM, Dollé P, Blanton SH, Northrup H. Mastrobattista JM, et al. Among authors: blanton sh. J Med Genet. 1995 Nov;32(11):851-4. doi: 10.1136/jmg.32.11.851. J Med Genet. 1995. PMID: 8592325 Free PMC article.

7

Report of a critical recombination further narrowing the TSC1 region.

Au KS, Murrell J, Buckler A, Blanton SH, Northrup H. Au KS, et al. Among authors: blanton sh. J Med Genet. 1996 Jul;33(7):559-61. doi: 10.1136/jmg.33.7.559. J Med Genet. 1996. PMID: 8818940 Free PMC article.

8

Linkage studies for markers on 9q to tuberous sclerosis.

Northrup H, Blanton SH. Northrup H, et al. Among authors: blanton sh. Ann N Y Acad Sci. 1991;615:384-5. doi: 10.1111/j.1749-6632.1991.tb37790.x. Ann N Y Acad Sci. 1991. PMID: 1674847 No abstract available.

9

Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability.

Volcik KA, Blanton SH, Northrup H. Volcik KA, et al. Among authors: blanton sh. Am J Hum Genet. 2001 Nov;69(5):1150-3. doi: 10.1086/324066. Am J Hum Genet. 2001. PMID: 11590551 Free PMC article. No abstract available.

10

Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere.

Northrup H, Kwiatkowski DJ, Roach ES, Dobyns WB, Lewis RA, Herman GE, Rodriguez E Jr, Daiger SP, Blanton SH. Northrup H, et al. Among authors: blanton sh. Am J Hum Genet. 1992 Oct;51(4):709-20. Am J Hum Genet. 1992. PMID: 1415216 Free PMC article.

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