Brothman AR - Search Results

1

Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients.

Lowery MC, Morris CA, Ewart A, Brothman LJ, Zhu XL, Leonard CO, Carey JC, Keating M, Brothman AR. Lowery MC, et al. Among authors: brothman lj, brothman ar. Am J Hum Genet. 1995 Jul;57(1):49-53. Am J Hum Genet. 1995. PMID: 7611295 Free PMC article.

2

Evaluation of 20 archival prostate tumor specimens by fluorescence in situ hybridization (FISH).

Brothman AR, Watson MJ, Zhu XL, Williams BJ, Rohr LR. Brothman AR, et al. Cancer Genet Cytogenet. 1994 Jul 1;75(1):40-4. doi: 10.1016/0165-4608(94)90213-5. Cancer Genet Cytogenet. 1994. PMID: 8039162

3

Cytogenetic and molecular analysis in trisomy 12p.

Allen TL, Brothman AR, Carey JC, Chance PF. Allen TL, et al. Among authors: brothman ar. Am J Med Genet. 1996 May 3;63(1):250-6. doi: 10.1002/(SICI)1096-8628(19960503)63:1<250::AID-AJMG43>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8723118 Review.

4

Partial trisomy 17p detected by spectral karyotyping.

Morelli SH, Deubler DA, Brothman LJ, Carey JC, Brothman AR. Morelli SH, et al. Among authors: brothman lj, brothman ar. Clin Genet. 1999 May;55(5):372-5. doi: 10.1034/j.1399-0004.1999.550513.x. Clin Genet. 1999. PMID: 10422810

5

4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotype.

Stevenson DA, Carey JC, Cowley BC, Bayrak-Toydemir P, Mao R, Brothman AR. Stevenson DA, et al. Among authors: brothman ar. J Pediatr. 2004 Dec;145(6):840-2. doi: 10.1016/j.jpeds.2004.08.027. J Pediatr. 2004. PMID: 15580214

6

Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations.

South ST, Whitby H, Battaglia A, Carey JC, Brothman AR. South ST, et al. Among authors: brothman ar. Eur J Hum Genet. 2008 Jan;16(1):45-52. doi: 10.1038/sj.ejhg.5201915. Epub 2007 Aug 29. Eur J Hum Genet. 2008. PMID: 17726485

7

Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.

South ST, Whitby H, Maxwell T, Aston E, Brothman AR, Carey JC. South ST, et al. Among authors: brothman ar. Am J Med Genet A. 2008 Oct 15;146A(20):2691-7. doi: 10.1002/ajmg.a.32516. Am J Med Genet A. 2008. PMID: 18798325

8

Aneusomy of chromosomes 7 and 17 detected by FISH in prostate cancer and the effects of selection in vitro.

Jones E, Zhu XL, Rohr LR, Stephenson RA, Brothman AR. Jones E, et al. Among authors: brothman ar. Genes Chromosomes Cancer. 1994 Nov;11(3):163-70. doi: 10.1002/gcc.2870110305. Genes Chromosomes Cancer. 1994. PMID: 7530485

9

Molecular cytogenetic analysis of a t(7;10) in a human glioblastoma cell line.

Fults D, Pedone CA, Zhu XL, Williams BJ, Jones E, Brothman AR. Fults D, et al. Among authors: brothman ar. Cancer Genet Cytogenet. 1995 Jun;81(2):118-24. doi: 10.1016/0165-4608(94)00265-d. Cancer Genet Cytogenet. 1995. PMID: 7621407

10

Multiple congenital anomalies in a man with (X;6) translocation.

Sivak LE, Esbenshade J, Brothman AR, Issa B, Lemons RS, Carey JC. Sivak LE, et al. Among authors: brothman ar. Am J Med Genet. 1994 May 15;51(1):9-12. doi: 10.1002/ajmg.1320510103. Am J Med Genet. 1994. PMID: 8030680

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