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

Year Number of Results
1974 1
1978 1
1983 1
1991 2
1993 1
1994 1
1995 1
2001 2
2005 1
2006 1
2012 3
2013 1
2015 1
2021 0
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17 results
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Page 1
Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing.
Merico D, Roifman M, Braunschweig U, Yuen RK, Alexandrova R, Bates A, Reid B, Nalpathamkalam T, Wang Z, Thiruvahindrapuram B, Gray P, Kakakios A, Peake J, Hogarth S, Manson D, Buncic R, Pereira SL, Herbrick JA, Blencowe BJ, Roifman CM, Scherer SW. Merico D, et al. Among authors: buncic r. Nat Commun. 2015 Nov 2;6:8718. doi: 10.1038/ncomms9718. Nat Commun. 2015. PMID: 26522830 Free PMC article.
Factors associated with strabismus in spina bifida myelomeningocele.
Anderson HA, Stuebing KK, Buncic R, Mazow M, Fletcher JM. Anderson HA, et al. Among authors: buncic r. J Pediatr Ophthalmol Strabismus. 2012 Sep-Oct;49(5):284-9. doi: 10.3928/01913913-20120501-01. Epub 2012 May 8. J Pediatr Ophthalmol Strabismus. 2012. PMID: 22588727 Free PMC article.
Primary hereditary oxalosis retinopathy.
Zak TA, Buncic R. Zak TA, et al. Among authors: buncic r. Arch Ophthalmol. 1983 Jan;101(1):78-80. doi: 10.1001/archopht.1983.01040010080013. Arch Ophthalmol. 1983. PMID: 6849658
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