Drumheller TC - Search Results

1

A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: fluorescence in situ hybridization and dosage-sensitive Southern blot analysis.

Gripp KW, Kasparcova V, McDonald-McGinn DM, Bhatt S, Bartlett SP, Storm AL, Drumheller TC, Emanuel BS, Zackai EH, Stolle CA. Gripp KW, et al. Among authors: drumheller tc. Genet Med. 2001 Mar-Apr;3(2):102-8. doi: 10.1097/00125817-200103000-00003. Genet Med. 2001. PMID: 11280946 Free article.

2

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

Drumheller T, McGillivray BC, Behrner D, MacLeod P, McFadden DE, Roberson J, Venditti C, Chorney K, Chorney M, Smith DI. Drumheller T, et al. J Med Genet. 1996 Oct;33(10):842-7. doi: 10.1136/jmg.33.10.842. J Med Genet. 1996. PMID: 8933338 Free PMC article.

3

Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature.

Powell CM, Taggart RT, Drumheller TC, Wangsa D, Qian C, Nelson LM, White BJ. Powell CM, et al. Among authors: drumheller tc. Am J Med Genet. 1994 Aug 1;52(1):19-26. doi: 10.1002/ajmg.1320520105. Am J Med Genet. 1994. PMID: 7977456 Review.

4

Chromosome 3p25 deletion in mother and daughter with minimal phenotypic effect.

Takagishi J, Rauen KA, Drumheller T, Kousseff B, Sutcliffe M. Takagishi J, et al. Am J Med Genet A. 2006 Jul 15;140(14):1587-93. doi: 10.1002/ajmg.a.31325. Am J Med Genet A. 2006. PMID: 16770804

5

Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster.

Del Campo M, Jones MC, Veraksa AN, Curry CJ, Jones KL, Mascarello JT, Ali-Kahn-Catts Z, Drumheller T, McGinnis W. Del Campo M, et al. Am J Hum Genet. 1999 Jul;65(1):104-10. doi: 10.1086/302467. Am J Hum Genet. 1999. PMID: 10364522 Free PMC article.

6

Identification of human chromosome region 3p14.2-21.3-specific YAC clones using Alu-PCR products from a radiation hybrid.

Siden TS, Kumlien J, Drumheller T, Smith SE, Röhme D, Lehrach H, Smith DI. Siden TS, et al. Somat Cell Mol Genet. 1994 Mar;20(2):137-42. doi: 10.1007/BF02290683. Somat Cell Mol Genet. 1994. PMID: 8009367

7

Recurrent cytogenetic abnormalities in squamous cell carcinomas of the head and neck region.

Van Dyke DL, Worsham MJ, Benninger MS, Krause CJ, Baker SR, Wolf GT, Drumheller T, Tilley BC, Carey TE. Van Dyke DL, et al. Genes Chromosomes Cancer. 1994 Mar;9(3):192-206. doi: 10.1002/gcc.2870090308. Genes Chromosomes Cancer. 1994. PMID: 7515662

8

Measurement of pesticides and other toxicants in amniotic fluid as a potential biomarker of prenatal exposure: a validation study.

Bradman A, Barr DB, Claus Henn BG, Drumheller T, Curry C, Eskenazi B. Bradman A, et al. Environ Health Perspect. 2003 Nov;111(14):1779-82. doi: 10.1289/ehp.6259. Environ Health Perspect. 2003. PMID: 14594631 Free PMC article.

9

Cytogenetic findings in pituitary adenoma: results of a pilot study.

Rock JP, Babu VR, Drumheller T, Chason J. Rock JP, et al. Surg Neurol. 1993 Sep;40(3):224-9. doi: 10.1016/0090-3019(93)90071-8. Surg Neurol. 1993. PMID: 8346476

10

Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkin's lymphoma: results of the FAB/LMB 96 international study.

Poirel HA, Cairo MS, Heerema NA, Swansbury J, Aupérin A, Launay E, Sanger WG, Talley P, Perkins SL, Raphaël M, McCarthy K, Sposto R, Gerrard M, Bernheim A, Patte C; FAB/LMB 96 International Study Committee. Poirel HA, et al. Leukemia. 2009 Feb;23(2):323-31. doi: 10.1038/leu.2008.312. Epub 2008 Nov 20. Leukemia. 2009. PMID: 19020548 Free PMC article.

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