Brothman AR - Search Results

1

Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platform.

Aston E, Whitby H, Maxwell T, Glaus N, Cowley B, Lowry D, Zhu XL, Issa B, South ST, Brothman AR. Aston E, et al. Among authors: brothman ar. J Med Genet. 2008 May;45(5):268-74. doi: 10.1136/jmg.2007.055319. Epub 2008 Jan 4. J Med Genet. 2008. PMID: 18178633

2

A new genomic mechanism leading to cri-du-chat syndrome.

South ST, Swensen JJ, Maxwell T, Rope A, Brothman AR, Chen Z. South ST, et al. Among authors: brothman ar. Am J Med Genet A. 2006 Dec 15;140(24):2714-20. doi: 10.1002/ajmg.a.31496. Am J Med Genet A. 2006. PMID: 17103439

3

Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.

Svensson AM, Curry CJ, South ST, Whitby H, Maxwell TM, Aston E, Fisher J, Carmack CE, Scheffer A, Abu-Shamsieh A, Brothman AR. Svensson AM, et al. Among authors: brothman ar. Am J Med Genet A. 2007 Jun 15;143A(12):1348-53. doi: 10.1002/ajmg.a.31775. Am J Med Genet A. 2007. PMID: 17506097

4

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

5

Genomic medicine in prenatal diagnosis.

South ST, Chen Z, Brothman AR. South ST, et al. Among authors: brothman ar. Clin Obstet Gynecol. 2008 Mar;51(1):62-73. doi: 10.1097/GRF.0b013e3181616509. Clin Obstet Gynecol. 2008. PMID: 18303500 Review.

6

How physicians use array comparative genomic hybridization results to guide patient management in children with developmental delay.

Saam J, Gudgeon J, Aston E, Brothman AR. Saam J, et al. Among authors: brothman ar. Genet Med. 2008 Mar;10(3):181-6. doi: 10.1097/GIM.0b013e3181634eca. Genet Med. 2008. PMID: 18344707 Free article.

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

Clinical laboratory implementation of cytogenomic microarrays.

South ST, Brothman AR. South ST, et al. Among authors: brothman ar. Cytogenet Genome Res. 2011;135(3-4):203-11. doi: 10.1159/000331425. Epub 2011 Sep 16. Cytogenet Genome Res. 2011. PMID: 21934287 Review.

9

Multiple abnormalities detected by dye reversal genomic microarrays in prostate cancer: a much greater sensitivity than conventional cytogenetics.

Pettus JA, Cowley BC, Maxwell T, Milash B, Stephenson RA, Rohr LR, Hoff C, Brothman AR. Pettus JA, et al. Among authors: brothman ar. Cancer Genet Cytogenet. 2004 Oct 15;154(2):110-8. doi: 10.1016/j.cancergencyto.2004.05.019. Cancer Genet Cytogenet. 2004. PMID: 15474145

10

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

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