Bleeker-Wagemakers EM - Search Results

1

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. Genomics. 1988 Apr;2(3):263-6. doi: 10.1016/0888-7543(88)90011-0. Genomics. 1988. PMID: 3397063

2

Golden tapetal reflex in male patients with X-linked retinitis pigmentosa. Case report and practical implications.

van Osch L, van Schooneveld M, Bleekerwagemakers EM. van Osch L, et al. Ophthalmic Paediatr Genet. 1990 Dec;11(4):287-91. doi: 10.3109/13816819009015715. Ophthalmic Paediatr Genet. 1990. PMID: 2096357

3

Posthumous diagnosis of X-linked retinoschisis using DNA analysis.

van Schooneveld MJ, Bleeker-Wagemakers EM, Orth U, Neugebauer M, Hogenkamp T, Gal A. van Schooneveld MJ, et al. Ophthalmic Paediatr Genet. 1990 Dec;11(4):293-7. doi: 10.3109/13816819009015716. Ophthalmic Paediatr Genet. 1990. PMID: 1982897

4

Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family.

van den Born LI, van Schooneveld MJ, de Jong LA, Riemslag FC, de Jong PT, Gal A, Bleeker-Wagemakers EM. van den Born LI, et al. Ophthalmic Genet. 1994 Jun;15(2):51-60. doi: 10.3109/13816819409098864. Ophthalmic Genet. 1994. PMID: 7850269

5

Autosomal recessive retinitis pigmentosa with preserved para-arteriolar retinal pigment epithelium.

van den Born LI, van Soest S, van Schooneveld MJ, Riemslag FC, de Jong PT, Bleeker-Wagemakers EM. van den Born LI, et al. Am J Ophthalmol. 1994 Oct 15;118(4):430-9. doi: 10.1016/s0002-9394(14)75792-7. Am J Ophthalmol. 1994. PMID: 7943119

6

Multipoint linkage analysis in X-linked juvenile retinoschisis.

Bergen AA, van Schooneveld MJ, Orth U, Bleeker-Wagemakers EM, Gal A. Bergen AA, et al. Clin Genet. 1993 Mar;43(3):113-6. doi: 10.1111/j.1399-0004.1993.tb04433.x. Clin Genet. 1993. PMID: 8500256

7

Fuchs' heterochromic uveitis associated with retinitis pigmentosa in a father and son.

van den Born LI, van Schooneveld MJ, de Jong PT, Bleeker-Wagemakers EM. van den Born LI, et al. Br J Ophthalmol. 1994 Jun;78(6):504-5. doi: 10.1136/bjo.78.6.504. Br J Ophthalmol. 1994. PMID: 8060947 Free PMC article. No abstract available.

8

Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis.

Bergen AA, Samanns C, Van Dorp DB, Ferguson-Smith MA, Gal A, Bleeker-Wagemakers EM. Bergen AA, et al. Ophthalmic Paediatr Genet. 1990 Sep;11(3):165-70. doi: 10.3109/13816819009020975. Ophthalmic Paediatr Genet. 1990. PMID: 2280973

9

Norrie disease as part of a complex syndrome explained by a submicroscopic deletion of the X chromosome.

Bleeker-Wagemakers EM, Zweije-Hofman I, Gal A. Bleeker-Wagemakers EM, et al. Ophthalmic Paediatr Genet. 1988 Nov;9(3):137-42. doi: 10.3109/13816818809031489. Ophthalmic Paediatr Genet. 1988. PMID: 3231429

10

X-linked megalocornea. Ocular findings and linkage analysis.

Meire FM, Bleeker-Wagemakers EM, Oehler M, Gal A, Delleman JW. Meire FM, et al. Ophthalmic Paediatr Genet. 1991 Sep;12(3):153-7. doi: 10.3109/13816819109029398. Ophthalmic Paediatr Genet. 1991. PMID: 1754164 Review.

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