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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1982 1
1983 1
1984 2
1985 2
1986 2
1987 2
1989 2
1990 3
1991 3
1992 4
1993 2
1994 6
1995 6
1996 6
1997 7
1998 5
1999 7
2000 4
2001 4
2002 4
2003 3
2004 5
2005 7
2006 3
2007 6
2008 8
2009 5
2010 3
2011 7
2012 2
2013 2
2014 1
2023 0
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122 results
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Page 1
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla JA, Eichler EE, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RM, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Miller DT, et al. Among authors: brothman ar. Am J Hum Genet. 2010 May 14;86(5):749-64. doi: 10.1016/j.ajhg.2010.04.006. Am J Hum Genet. 2010. PMID: 20466091 Free PMC article. Review.
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, Collinson MN, Beal SJ, Ackley T, Pickering DL, Golden DM, Aston E, Whitby H, Shetty S, Rossi MR, Rudd MK, South ST, Brothman AR, Sanger WG, Iyer RK, Crolla JA, Thorland EC, Aradhya S, Ledbetter DH, Martin CL. Kaminsky EB, et al. Among authors: brothman ar. Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9. Genet Med. 2011. PMID: 21844811 Free PMC article.
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.
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.
Microarray analysis for constitutional cytogenetic abnormalities.
Shaffer LG, Beaudet AL, Brothman AR, Hirsch B, Levy B, Martin CL, Mascarello JT, Rao KW; Working Group of the Laboratory Quality Assurance Committee of the American College of Medical Genetics. Shaffer LG, et al. Among authors: brothman ar. Genet Med. 2007 Sep;9(9):654-62. doi: 10.1097/gim.0b013e31814ce3d9. Genet Med. 2007. PMID: 17873655 No abstract available.
Familial ring (19) chromosome mosaicism: case report and review.
Flejter WL, Finlinson D, Root S, Nguyen W, Brothman AR, Viskochil D. Flejter WL, et al. Among authors: brothman ar. Am J Med Genet. 1996 Dec 18;66(3):276-80. doi: 10.1002/(SICI)1096-8628(19961218)66:3<276::AID-AJMG8>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8985487 Review.
122 results