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

Year Number of Results
1973 1
1982 1
1987 2
1988 3
1990 3
1991 3
1992 2
1993 1
1996 1
1997 1
1998 1
1999 2
2000 1
2001 1
2003 1
2004 1
2005 2
2006 2
2007 1
2008 1
2011 1
2012 5
2013 1
2014 2
2016 1
2017 3
2018 1
2019 2
2020 1
2021 1
2024 0

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48 results

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Page 1
Inherited 2q23.1 microdeletions involving the MBD5 locus.
Tadros S, Wang R, Waters JJ, Waterman C, Collins AL, Collinson MN, Ahn JW, Josifova D, Chetan R, Kumar A. Tadros S, et al. Among authors: waters jj. Mol Genet Genomic Med. 2017 Aug 8;5(5):608-613. doi: 10.1002/mgg3.316. eCollection 2017 Sep. Mol Genet Genomic Med. 2017. PMID: 28944244 Free PMC article.
Characterization of LysBC17, a Lytic Endopeptidase from Bacillus cereus.
Swift SM, Etobayeva IV, Reid KP, Waters JJ, Oakley BB, Donovan DM, Nelson DC. Swift SM, et al. Among authors: waters jj. Antibiotics (Basel). 2019 Sep 19;8(3):155. doi: 10.3390/antibiotics8030155. Antibiotics (Basel). 2019. PMID: 31546935 Free PMC article.
Demystified ... FISH.
Waters JJ, Barlow AL, Gould CP. Waters JJ, et al. Mol Pathol. 1998 Apr;51(2):62-70. doi: 10.1136/mp.51.2.62. Mol Pathol. 1998. PMID: 9713588 Free PMC article. Review. No abstract available.
Diagnostic implications of genetic copy number variation in epilepsy plus.
Coppola A, Cellini E, Stamberger H, Saarentaus E, Cetica V, Lal D, Djémié T, Bartnik-Glaska M, Ceulemans B, Helen Cross J, Deconinck T, Masi S, Dorn T, Guerrini R, Hoffman-Zacharska D, Kooy F, Lagae L, Lench N, Lemke JR, Lucenteforte E, Madia F, Mefford HC, Morrogh D, Nuernberg P, Palotie A, Schoonjans AS, Striano P, Szczepanik E, Tostevin A, Vermeesch JR, Van Esch H, Van Paesschen W, Waters JJ, Weckhuysen S, Zara F, De Jonghe P, Sisodiya SM, Marini C; EuroEPINOMICS-RES Consortium; EpiCNV Consortium. Coppola A, et al. Among authors: waters jj. Epilepsia. 2019 Apr;60(4):689-706. doi: 10.1111/epi.14683. Epub 2019 Mar 13. Epilepsia. 2019. PMID: 30866059 Free PMC article.
The principles of clinical cytogenetics.
Waters JJ. Waters JJ. J Med Genet. 2000 May;37(5):399. doi: 10.1136/jmg.37.5.399. J Med Genet. 2000. PMID: 10807698 Free PMC article. No abstract available.
The idic(15) syndrome: expanding the phenotype.
Galizia EC, Palmer R, Waters JJ, Koepp MJ, Hennekam RC, Sisodiya SM. Galizia EC, et al. Among authors: waters jj. Am J Med Genet A. 2012 Jun;158A(6):1505-8. doi: 10.1002/ajmg.a.35366. Epub 2012 May 14. Am J Med Genet A. 2012. PMID: 22585586 No abstract available.
A Novel Variant in the TBC1D24 Lipid-Binding Pocket Causes Autosomal Dominant Hearing Loss: Evidence for a Genotype-Phenotype Correlation.
Parzefall T, Frohne A, Koenighofer M, Neesen J, Laccone F, Eckl-Dorna J, Waters JJ, Schreiner M, Amr SS, Ashton E, Schoefer C, Gstœttner W, Frei K, Lucas T. Parzefall T, et al. Among authors: waters jj. Front Cell Neurosci. 2020 Nov 12;14:585669. doi: 10.3389/fncel.2020.585669. eCollection 2020. Front Cell Neurosci. 2020. PMID: 33281559 Free PMC article.
48 results