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Results by year

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

Year Number of Results
1963 1
1967 2
1968 3
1971 2
1972 3
1976 1
1977 2
1979 3
1980 6
1981 3
1982 4
1983 6
1984 7
1985 1
1986 7
1987 11
1988 1
1989 4
1990 6
1991 9
1992 15
1993 13
1994 5
1995 1
1996 10
1997 5
1998 5
1999 11
2000 11
2001 7
2002 6
2003 6
2004 4
2005 4
2006 3
2007 3
2008 5
2009 3
2010 1
2011 2
2012 2
2013 1
2014 2
2015 1
2016 1
2017 2
2018 1
2024 0

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Article type

Publication date

PubMed (OMIM) for id: 791114

205 results

Results by year

Filters applied: . Clear all
Page 1
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. Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9. Genet Med. 2011. PMID: 21844811 Free PMC article.
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism.
de Smith AJ, Purmann C, Walters RG, Ellis RJ, Holder SE, Van Haelst MM, Brady AF, Fairbrother UL, Dattani M, Keogh JM, Henning E, Yeo GS, O'Rahilly S, Froguel P, Farooqi IS, Blakemore AI. de Smith AJ, et al. Hum Mol Genet. 2009 Sep 1;18(17):3257-65. doi: 10.1093/hmg/ddp263. Epub 2009 Jun 4. Hum Mol Genet. 2009. PMID: 19498035 Free PMC article.
205 results