Bodurtha J - Search Results

1

Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10.

Rampersaud E, Bassuk AG, Enterline DS, George TM, Siegel DG, Melvin EC, Aben J, Allen J, Aylsworth A, Brei T, Bodurtha J, Buran C, Floyd LE, Hammock P, Iskandar B, Ito J, Kessler JA, Lasarsky N, Mack P, Mackey J, McLone D, Meeropol E, Mehltretter L, Mitchell LE, Oakes WJ, Nye JS, Powell C, Sawin K, Stevenson R, Walker M, West SG, Worley G, Gilbert JR, Speer MC. Rampersaud E, et al. Among authors: bodurtha j. J Med Genet. 2005 Dec;42(12):940-6. doi: 10.1136/jmg.2005.031658. Epub 2005 Apr 14. J Med Genet. 2005. PMID: 15831595 Free PMC article.

2

College women's awareness and consumption of folic acid for the prevention of neural tube defects.

Quillin JM, Silberg J, Board P, Pratt L, Bodurtha J. Quillin JM, et al. Among authors: bodurtha j. Genet Med. 2000 Jul-Aug;2(4):209-13. doi: 10.1097/00125817-200007000-00002. Genet Med. 2000. PMID: 11252704 Free article.

3

A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

Osborne LR, Li M, Pober B, Chitayat D, Bodurtha J, Mandel A, Costa T, Grebe T, Cox S, Tsui LC, Scherer SW. Osborne LR, et al. Among authors: bodurtha j. Nat Genet. 2001 Nov;29(3):321-5. doi: 10.1038/ng753. Nat Genet. 2001. PMID: 11685205 Free PMC article.

4

Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation.

Tekin M, Jackson-Cook C, Buller A, Ferreira-Gonzalez A, Pandya A, Garrett CT, Bodurtha J. Tekin M, et al. Among authors: bodurtha j. Am J Med Genet. 2000 Nov 13;95(2):145-9. doi: 10.1002/1096-8628(20001113)95:2<145::aid-ajmg10>3.0.co;2-r. Am J Med Genet. 2000. PMID: 11078565

5

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.

Marsh DJ, Kum JB, Lunetta KL, Bennett MJ, Gorlin RJ, Ahmed SF, Bodurtha J, Crowe C, Curtis MA, Dasouki M, Dunn T, Feit H, Geraghty MT, Graham JM Jr, Hodgson SV, Hunter A, Korf BR, Manchester D, Miesfeldt S, Murday VA, Nathanson KL, Parisi M, Pober B, Romano C, Eng C, et al. Marsh DJ, et al. Among authors: bodurtha j. Hum Mol Genet. 1999 Aug;8(8):1461-72. doi: 10.1093/hmg/8.8.1461. Hum Mol Genet. 1999. PMID: 10400993

6

Analysis of variability of clinical manifestations in Waardenburg syndrome.

Reynolds JE, Meyer JM, Landa B, Stevens CA, Arnos KS, Israel J, Marazita ML, Bodurtha J, Nance WE, Diehl SR. Reynolds JE, et al. Among authors: bodurtha j. Am J Med Genet. 1995 Jul 17;57(4):540-7. doi: 10.1002/ajmg.1320570405. Am J Med Genet. 1995. PMID: 7573125

7

Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study.

Fleck BJ, Pandya A, Vanner L, Kerkering K, Bodurtha J. Fleck BJ, et al. Among authors: bodurtha j. Am J Med Genet. 2001 Feb 15;99(1):1-7. doi: 10.1002/1096-8628(20010215)99:1<1::aid-ajmg1127>3.0.co;2-a. Am J Med Genet. 2001. PMID: 11170086 Review.

8

Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature.

Garganta CL, Bodurtha JN. Garganta CL, et al. Among authors: bodurtha jn. Am J Med Genet. 1992 Sep 15;44(2):129-35. doi: 10.1002/ajmg.1320440202. Am J Med Genet. 1992. PMID: 1456279 Review.

9

Evidence for a major gene in familial anencephaly.

Shaffer LG, Marazita ML, Bodurtha J, Newlin A, Nance WE. Shaffer LG, et al. Among authors: bodurtha j. Am J Med Genet. 1990 May;36(1):97-101. doi: 10.1002/ajmg.1320360119. Am J Med Genet. 1990. PMID: 2333913

10

The risk of neural tube defects to first cousins of affected individuals.

Zackai EH, Spielman RS, Mellman WJ, Ames M, Bodurtha J. Zackai EH, et al. Among authors: bodurtha j. UCLA Forum Med Sci. 1978;20:99-102. UCLA Forum Med Sci. 1978. PMID: 695015 No abstract available.

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