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

Year Number of Results
1983 1
1984 1
1985 1
2004 1
2007 2
2008 1
2009 1
2015 1
2016 1
2017 2
2019 2
2020 1
2022 0
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12 results
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Page 1
Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalities.
Cipriani V, Kalhoro A, Arno G, Silva RS, Pontikos N, Puech V, McClements ME, Hunt DM, van Heyningen V, Michaelides M, Webster AR, Moore AT, Puech B. Cipriani V, et al. Among authors: kalhoro a. Ophthalmic Genet. 2017 Dec;38(6):511-519. doi: 10.1080/13816810.2017.1289544. Epub 2017 Mar 2. Ophthalmic Genet. 2017. PMID: 28635424 Free article.
Unique noncoding variants upstream of PRDM13 are associated with a spectrum of developmental retinal dystrophies including progressive bifocal chorioretinal atrophy.
Silva RS, Arno G, Cipriani V, Pontikos N, Defoort-Dhellemmes S, Kalhoro A, Carss KJ, Raymond FL, Dhaenens CM, Jensen H, Rosenberg T, van Heyningen V, Moore AT, Puech B, Webster AR. Silva RS, et al. Among authors: kalhoro a. Hum Mutat. 2019 May;40(5):578-587. doi: 10.1002/humu.23715. Epub 2019 Feb 14. Hum Mutat. 2019. PMID: 30710461
Diaphragmatic rupture in a mare at parturition.
Auer DE, Wilson RG, Groenendyk S, Kalhoro A, Wilson RP. Auer DE, et al. Among authors: kalhoro a. Equine Vet J. 1985 Jul;17(4):331-3. doi: 10.1111/j.2042-3306.1985.tb02512.x. Equine Vet J. 1985. PMID: 4076151 No abstract available.
Juvenile Batten Disease (CLN3): Detailed Ocular Phenotype, Novel Observations, Delayed Diagnosis, Masquerades, and Prospects for Therapy.
Wright GA, Georgiou M, Robson AG, Ali N, Kalhoro A, Holthaus SK, Pontikos N, Oluonye N, de Carvalho ER, Neveu MM, Weleber RG, Michaelides M. Wright GA, et al. Among authors: kalhoro a. Ophthalmol Retina. 2020 Apr;4(4):433-445. doi: 10.1016/j.oret.2019.11.005. Epub 2019 Nov 13. Ophthalmol Retina. 2020. PMID: 31926949 Free PMC article.
12 results