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

Year Number of Results
1971 1
1976 1
1977 2
1978 1
1979 1
1980 1
1984 2
1986 2
1987 5
1988 3
1989 3
1990 5
1991 6
1992 6
1993 6
1994 6
1995 5
1996 3
1997 3
1998 2
1999 3
2022 0
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67 results
Results by year
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Page 1
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: bleeker wagemakers em. Ophthalmic Paediatr Genet. 1991 Sep;12(3):153-7. doi: 10.3109/13816819109029398. Ophthalmic Paediatr Genet. 1991. PMID: 1754164 Review.
Retinitis pigmentosa: defined from a molecular point of view.
van Soest S, Westerveld A, de Jong PT, Bleeker-Wagemakers EM, Bergen AA. van Soest S, et al. Among authors: bleeker wagemakers em. Surv Ophthalmol. 1999 Jan-Feb;43(4):321-34. doi: 10.1016/s0039-6257(98)00046-0. Surv Ophthalmol. 1999. PMID: 10025514 Review.
Molecular basis of choroideremia (CHM): mutations involving the Rab escort protein-1 (REP-1) gene.
van den Hurk JA, Schwartz M, van Bokhoven H, van de Pol TJ, Bogerd L, Pinckers AJ, Bleeker-Wagemakers EM, Pawlowitzki IH, Rüther K, Ropers HH, Cremers FP. van den Hurk JA, et al. Among authors: bleeker wagemakers em. Hum Mutat. 1997;9(2):110-7. doi: 10.1002/(SICI)1098-1004(1997)9:2<110::AID-HUMU2>3.0.CO;2-D. Hum Mutat. 1997. PMID: 9067750 Free article. Review.
Peters'-plus: a new syndrome.
van Schooneveld MJ, Delleman JW, Beemer FA, Bleeker-Wagemakers EM. van Schooneveld MJ, et al. Among authors: bleeker wagemakers em. Ophthalmic Paediatr Genet. 1984 Dec;4(3):141-5. doi: 10.3109/13816818409006113. Ophthalmic Paediatr Genet. 1984. PMID: 6443615
Ophthalmologic findings in Usher syndrome type 2A.
Van Aarem A, Wagenaar M, Pinckers AJ, Huygen PL, Bleeker-Wagemakers EM, Kimberling BJ, Cremers CW. Van Aarem A, et al. Among authors: bleeker wagemakers em. Ophthalmic Genet. 1995 Dec;16(4):151-8. doi: 10.3109/13816819509057856. Ophthalmic Genet. 1995. PMID: 8749051
Two different genes for X-linked retinitis pigmentosa.
Wirth B, Denton MJ, Chen JD, Neugebauer M, Halliday FB, van Schooneveld M, Donald J, Bleeker-Wagemakers EM, Pearson PL, Gal A. Wirth B, et al. Among authors: bleeker wagemakers em. Genomics. 1988 Apr;2(3):263-6. doi: 10.1016/0888-7543(88)90011-0. Genomics. 1988. PMID: 3397063
Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis).
Taschner PE, de Vos N, Post JG, Meijers-Heijboer EJ, Hofman I, Loonen MC, Pinckers AJ, Bleeker-Wagemakers EM, Gardiner RM, Breuning MH. Taschner PE, et al. Among authors: bleeker wagemakers em. Am J Med Genet. 1995 Jun 5;57(2):333-7. doi: 10.1002/ajmg.1320570246. Am J Med Genet. 1995. PMID: 7668358 Free article.
[Heredity in ophthalmology].
Delleman JW, Bleeker-Wagemakers EM, van Schooneveld MJ. Delleman JW, et al. Among authors: bleeker wagemakers em. Ned Tijdschr Geneeskd. 1987 Dec 5;131(49):2226-30. Ned Tijdschr Geneeskd. 1987. PMID: 3696248 Dutch. No abstract available.
Prevalence of mental retardation in patients with hereditary retinoblastoma.
Moll AC, Imhof SM, Bleeker-Wagemakers EM, Den Otter W, Bouter LM, Koten JW, Tan KE. Moll AC, et al. Among authors: bleeker wagemakers em. Ophthalmic Genet. 1997 Dec;18(4):217-20. doi: 10.3109/13816819709041437. Ophthalmic Genet. 1997. PMID: 9457753 No abstract available.
The distal region of 11p13 and associated genetic diseases.
Mannens M, Hoovers JM, Bleeker-Wagemakers EM, Redeker E, Bliek J, Overbeeke-Melkert M, Saunders G, Williams B, van Heyningen V, Junien C, et al. Mannens M, et al. Among authors: bleeker wagemakers em. Genomics. 1991 Oct;11(2):284-93. doi: 10.1016/0888-7543(91)90134-z. Genomics. 1991. PMID: 1769647
67 results