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

Year Number of Results
1950 1
1968 1
1969 2
1970 3
1971 1
1972 1
1973 1
1975 1
1976 2
1977 5
1978 3
1979 2
1980 3
1981 1
1982 1
1983 4
1984 4
1985 2
1986 5
1987 5
1988 2
1990 1
1991 1
1992 1
1993 2
1994 4
1998 1
2022 0
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Article type
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Search Results

60 results
Results by year
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Page 1
Heterogeneity in Waardenburg syndrome.
Hageman MJ, Delleman JW. Hageman MJ, et al. Among authors: delleman jw. Am J Hum Genet. 1977 Sep;29(5):468-85. Am J Hum Genet. 1977. PMID: 331943 Free PMC article. Review.
ICE syndrome.
Begas AM, Delleman JW. Begas AM, et al. Among authors: delleman jw. Clin Genet. 1988 Jan;33(1):63. doi: 10.1111/j.1399-0004.1988.tb04268.x. Clin Genet. 1988. PMID: 3342550 No abstract available.
Hypertelorism in neurofibromatosis.
Wolters EC, Westerhof W, Delleman JW, Dijkstra P. Wolters EC, et al. Among authors: delleman jw. Neuropediatrics. 1986 Nov;17(4):175-7. doi: 10.1055/s-2008-1052523. Neuropediatrics. 1986. PMID: 3100978
X-linked megalocornea. Ocular findings and linkage analysis.
Meire FM, Bleeker-Wagemakers EM, Oehler M, Gal A, Delleman JW. Meire FM, et al. Among authors: delleman jw. Ophthalmic Paediatr Genet. 1991 Sep;12(3):153-7. doi: 10.3109/13816819109029398. Ophthalmic Paediatr Genet. 1991. PMID: 1754164 Review.
[Reis-Bücklers corneal dystrophy].
Winkelman JE, Wittebol-Post D, Delleman JW. Winkelman JE, et al. Among authors: delleman jw. Klin Monbl Augenheilkd. 1986 Feb;188(2):143-7. doi: 10.1055/s-2008-1050600. Klin Monbl Augenheilkd. 1986. PMID: 3520120 German.
Neurofibromatosis and hypertelorism.
Westerhof W, Delleman JW, Wolters E, Dijkstra P. Westerhof W, et al. Among authors: delleman jw. Arch Dermatol. 1984 Dec;120(12):1579-81. Arch Dermatol. 1984. PMID: 6439124
Albinism: phenotype or genotype?
van Dorp DB, van Haeringen NJ, Delleman JW, Apkarian P, Westerhof W. van Dorp DB, et al. Among authors: delleman jw. Doc Ophthalmol. 1983 Dec 15;56(1-2):183-94. doi: 10.1007/BF00154728. Doc Ophthalmol. 1983. PMID: 6420133
Peters'-plus: a new syndrome.
van Schooneveld MJ, Delleman JW, Beemer FA, Bleeker-Wagemakers EM. van Schooneveld MJ, et al. Among authors: delleman jw. Ophthalmic Paediatr Genet. 1984 Dec;4(3):141-5. doi: 10.3109/13816818409006113. Ophthalmic Paediatr Genet. 1984. PMID: 6443615
Goniodysgenesis in familial primary open-angle glaucoma.
Verbraak FD, vd Berg W, Delleman JW, Greve EL. Verbraak FD, et al. Among authors: delleman jw. Acta Ophthalmol (Copenh). 1994 Feb;72(1):98-102. doi: 10.1111/j.1755-3768.1994.tb02745.x. Acta Ophthalmol (Copenh). 1994. PMID: 8017205
Mental retardation in amaurosis congenita of Leber.
Schuil J, Meire FM, Delleman JW. Schuil J, et al. Among authors: delleman jw. Neuropediatrics. 1998 Dec;29(6):294-7. doi: 10.1055/s-2007-973580. Neuropediatrics. 1998. PMID: 10029347
60 results