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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1971 | 1 |
1982 | 1 |
1987 | 1 |
1997 | 1 |
2021 | 1 |
2024 | 0 |
PubMed for id: 868092
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Page 1
CHORIORETINAL CHANGES IN A GENETICALLY CONFIRMED CASE OF BOUCHER-NEUHÄUSER SYNDROME.
Retin Cases Brief Rep. 2021 Mar 1;15(2):179-184. doi: 10.1097/ICB.0000000000000769.
Retin Cases Brief Rep. 2021.
PMID: 30015775
Free PMC article.
Autosomal dominant vitreoretinochoroidopathy.
Roider J, Fritsch E, Hoerauf H, Heide W, Laqua H.
Roider J, et al.
Retina. 1997;17(4):294-9. doi: 10.1097/00006982-199707000-00003.
Retina. 1997.
PMID: 9279944
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Autosomal dominant vitreoretinochoroidopathy.
Kaufman SJ, Goldberg MF, Orth DH, Fishman GA, Tessler H, Mizuno K.
Kaufman SJ, et al.
Arch Ophthalmol. 1982 Feb;100(2):272-8. doi: 10.1001/archopht.1982.01030030274008.
Arch Ophthalmol. 1982.
PMID: 7065944
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Sex-linked chorioretinal heredodegenerations.
François J.
François J.
Birth Defects Orig Artic Ser. 1971 Mar;7(3):99-116.
Birth Defects Orig Artic Ser. 1971.
PMID: 4950918
Review.
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Enhanced integumental and ocular amelanosis following the termination of cyclosporine administration.
Pardue SL, Fite KV, Bengston L, Lamont SJ, Boyle ML 3rd, Smyth JR Jr.
Pardue SL, et al.
J Invest Dermatol. 1987 Jun;88(6):758-61. doi: 10.1111/1523-1747.ep12470453.
J Invest Dermatol. 1987.
PMID: 3585059
Free article.
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