van Schooneveld MJ - 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: van schooneveld mj. 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

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

3

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

4

Rieger's eye anomaly and persistent hyperplastic primary vitreous.

Storimans CW, Van Schooneveld MJ. Storimans CW, et al. Among authors: van schooneveld mj. Ophthalmic Paediatr Genet. 1989 Dec;10(4):257-62. doi: 10.3109/13816818909009880. Ophthalmic Paediatr Genet. 1989. PMID: 2628817

5

Peters' anomaly and systemic defects.

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

6

Efficient DNA carrier detection in X linked juvenile retinoschisis.

Bergen AA, ten Brink JB, van Schooneveld MJ. Bergen AA, et al. Among authors: van schooneveld mj. Br J Ophthalmol. 1995 Jul;79(7):683-6. doi: 10.1136/bjo.79.7.683. Br J Ophthalmol. 1995. PMID: 7662636 Free PMC article.

7

Fundus albipunctatus-like lesions in juvenile retinoschisis.

van Schooneveld MJ, Miyake Y. van Schooneveld MJ, et al. Br J Ophthalmol. 1994 Aug;78(8):659-61. doi: 10.1136/bjo.78.8.659. Br J Ophthalmol. 1994. PMID: 7918299 Free PMC article. No abstract available.

8

A submicroscopic deletion in a patient with isolated X-linked ocular albinism (OA1).

Bassi MT, Bergen AA, Wapenaar MC, Schiaffino MV, van Schooneveld M, Yates JR, Charles SJ, Meitinger T, Ballabio A. Bassi MT, et al. Hum Mol Genet. 1994 Apr;3(4):647-8. doi: 10.1093/hmg/3.4.647. Hum Mol Genet. 1994. PMID: 8069311 No abstract available.

9

Multipoint linkage analysis in X-linked juvenile retinoschisis.

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

10

Further delineation of the acro-renal-ocular syndrome.

Aalfs CM, van Schooneveld MJ, van Keulen EM, Hennekam RC. Aalfs CM, et al. Among authors: van schooneveld mj, van keulen em. Am J Med Genet. 1996 Mar 29;62(3):276-81. doi: 10.1002/(SICI)1096-8628(19960329)62:3<276::AID-AJMG14>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8882787

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