Bleeker-Wagemakers LM - Search Results

1

Refinement of the chromosomal position of the X linked juvenile retinoschisis gene.

Bergen AA, ten Brink JB, Bleeker-Wagemakers LM, van Schooneveld MJ. Bergen AA, et al. Among authors: bleeker wagemakers lm. J Med Genet. 1994 Dec;31(12):972-5. doi: 10.1136/jmg.31.12.972. J Med Genet. 1994. PMID: 7891384 Free PMC article.

2

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population.

van Soest S, van den Born LI, Gal A, Farrar GJ, Bleeker-Wagemakers LM, Westerveld A, Humphries P, Sandkuijl LA, Bergen AA. van Soest S, et al. Among authors: bleeker wagemakers lm. Genomics. 1994 Aug;22(3):499-504. doi: 10.1006/geno.1994.1422. Genomics. 1994. PMID: 8001962

3

Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1.

Roepman R, van Duijnhoven G, Rosenberg T, Pinckers AJ, Bleeker-Wagemakers LM, Bergen AA, Post J, Beck A, Reinhardt R, Ropers HH, Cremers FP, Berger W. Roepman R, et al. Among authors: bleeker wagemakers lm. Hum Mol Genet. 1996 Jul;5(7):1035-41. doi: 10.1093/hmg/5.7.1035. Hum Mol Genet. 1996. PMID: 8817343

4

Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa.

Bleeker-Wagemakers LM, Gal A, Kumar-Singh R, van den Born LI, Li Y, Schwinger E, Sandkuijl LA, Bergen AA, Kenna P, Humphries P, et al. Bleeker-Wagemakers LM, et al. Genomics. 1992 Nov;14(3):811-2. doi: 10.1016/s0888-7543(05)80195-8. Genomics. 1992. PMID: 1427914

5

Peters' anomaly and systemic defects.

van Schooneveld MJ, Delleman JW, Beemer FA, Bleeker-Wagemakers LM. van Schooneveld MJ, et al. Among authors: bleeker wagemakers lm. Arch Ophthalmol. 1986 Aug;104(8):1130. doi: 10.1001/archopht.1986.01050200036031. Arch Ophthalmol. 1986. PMID: 3741236 No abstract available.

6

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp.

Gal A, Schinzel A, Orth U, Fraser NA, Mollica F, Craig IW, Kruse T, Mächler M, Neugebauer M, Bleeker-Wagemakers LM. Gal A, et al. Among authors: bleeker wagemakers lm. Hum Genet. 1989 Mar;81(4):315-8. doi: 10.1007/BF00283682. Hum Genet. 1989. PMID: 2564836

7

Mutations in the candidate gene for Norrie disease.

Berger W, van de Pol D, Warburg M, Gal A, Bleeker-Wagemakers L, de Silva H, Meindl A, Meitinger T, Cremers F, Ropers HH. Berger W, et al. Hum Mol Genet. 1992 Oct;1(7):461-5. doi: 10.1093/hmg/1.7.461. Hum Mol Genet. 1992. PMID: 1307245 Review.

8

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.

Bleeker-Wagemakers LM, Friedrich U, Gal A, Wienker TF, Warburg M, Ropers HH. Bleeker-Wagemakers LM, et al. Hum Genet. 1985;71(3):211-4. doi: 10.1007/BF00284575. Hum Genet. 1985. PMID: 2998969

9

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease.

Gal A, Wieringa B, Smeets DF, Bleeker-Wagemakers L, Ropers HH. Gal A, et al. Cytogenet Cell Genet. 1986;42(4):219-24. doi: 10.1159/000132282. Cytogenet Cell Genet. 1986. PMID: 3502689

10

Oculocerebrocutaneous syndrome.

Bleeker-Wagemakers LM, Hamel BC, Hennekam RC, Beemer FA, Oorthuys HW. Bleeker-Wagemakers LM, et al. J Med Genet. 1990 Jan;27(1):69-70. doi: 10.1136/jmg.27.1.69. J Med Genet. 1990. PMID: 2407849 Free PMC article. Review. No abstract available.

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