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

Year Number of Results
1974 3
1976 2
1979 1
1980 1
1981 1
1985 1
1986 1
1988 2
1989 4
1990 3
1991 2
1992 3
1993 4
1994 1
1995 9
1996 8
1997 4
1998 5
1999 3
2000 3
2001 1
2002 2
2003 5
2004 2
2005 8
2006 3
2007 4
2008 9
2009 4
2010 10
2011 7
2012 5
2013 4
2014 3
2017 1
2018 1
2024 0

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126 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: crolla ja. 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: crolla ja. Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9. Genet Med. 2011. PMID: 21844811 Free PMC article.
Newton E. Morton (1929-2018).
Sherman SL, Rao DC, Keats BJ, Yee S, Spence MA, Hassold TJ, Chakravarti A, Elston RC, Crolla JA, Ennis S, Risch N. Sherman SL, et al. Among authors: crolla ja. Am J Hum Genet. 2018 Jun 7;102(6):1011-1017. doi: 10.1016/j.ajhg.2018.05.005. Epub 2018 Jun 8. Am J Hum Genet. 2018. PMID: 33220219 Free PMC article. No abstract available.
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.
Warburton PE, Dolled M, Mahmood R, Alonso A, Li S, Naritomi K, Tohma T, Nagai T, Hasegawa T, Ohashi H, Govaerts LC, Eussen BH, Van Hemel JO, Lozzio C, Schwartz S, Dowhanick-Morrissette JJ, Spinner NB, Rivera H, Crolla JA, Yu C, Warburton D. Warburton PE, et al. Among authors: crolla ja. Am J Hum Genet. 2000 Jun;66(6):1794-806. doi: 10.1086/302924. Epub 2000 Apr 24. Am J Hum Genet. 2000. PMID: 10777715 Free PMC article. Review.
Intrachromosomal triplication of distal 7p.
Rivera H, Bobadilla L, Rolon A, Kunz J, Crolla JA. Rivera H, et al. Among authors: crolla ja. J Med Genet. 1998 Jan;35(1):78-80. doi: 10.1136/jmg.35.1.78. J Med Genet. 1998. PMID: 9475103 Free PMC article.
Complex chromosomal rearrangements.
Creasy MR, Crolla JA. Creasy MR, et al. Among authors: crolla ja. Clin Genet. 1981 Jun;19(6):481-2. doi: 10.1111/j.1399-0004.1981.tb02068.x. Clin Genet. 1981. PMID: 7296941 No abstract available.
Clinical utility gene card for: WAGR syndrome.
Clericuzio C, Hingorani M, Crolla JA, van Heyningen V, Verloes A. Clericuzio C, et al. Among authors: crolla ja. Eur J Hum Genet. 2011 Apr;19(4). doi: 10.1038/ejhg.2010.220. Epub 2011 Jan 12. Eur J Hum Genet. 2011. PMID: 21224893 Free PMC article. No abstract available.
126 results