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

Year Number of Results
1998 1
2000 1
2001 1
2002 2
2003 1
2004 2
2005 1
2006 1
2009 1
2011 2
2013 1
2014 1
2017 1
2018 2
2019 2
2020 0
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18 results
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Page 1
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity.
de Crecchio G, Simonelli F, Nunziata G, Mazzeo S, Greco GM, Rinaldi E, Ventruto V, Ciccodicola A, Miano MG, Testa F, Curci A, D'Urso M, Rinaldi MM, Cavaliere ML, Castelluccio P. de Crecchio G, et al. Clin Genet. 1998 Oct;54(4):315-20. doi: 10.1034/j.1399-0004.1998.5440409.x. Clin Genet. 1998. PMID: 9831343
Wnt Signaling in vascular eye diseases.
Wang Z, Liu CH, Huang S, Chen J. Wang Z, et al. Prog Retin Eye Res. 2019 May;70:110-133. doi: 10.1016/j.preteyeres.2018.11.008. Epub 2018 Dec 1. Prog Retin Eye Res. 2019. PMID: 30513356 Review.
Molecular and clinical studies of X-linked deafness among Pakistani families.
Waryah AM, Ahmed ZM, Bhinder MA, Choo DI, Sisk RA, Shahzad M, Khan SN, Friedman TB, Riazuddin S, Riazuddin S. Waryah AM, et al. J Hum Genet. 2011 Jul;56(7):534-40. doi: 10.1038/jhg.2011.55. Epub 2011 Jun 2. J Hum Genet. 2011. PMID: 21633365 Free PMC article.
LRP5 sequence and polymorphisms in the baboon.
Doubleday AF, Kaestle FA, Cox LA, Birnbaum S, Mahaney MC, Havill LM. Doubleday AF, et al. J Med Primatol. 2009 Apr;38(2):97-106. doi: 10.1111/j.1600-0684.2008.00317.x. J Med Primatol. 2009. PMID: 19367734 Free PMC article.
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