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E J Schuurman

Showing results (1-10 of 11) with videos related to

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Clinical Genetics|May 1, 1994
DNA carrier detection in X-linked progressive cone dystrophyA A Bergen, F Meire, E J Schuurman, et al.
Genomics|May 1, 1994
Nance-Horan syndrome: linkage analysis in a family from The NetherlandsA A Bergen, J ten Brink, E J Schuurman, et al.
Human Molecular Genetics|May 1, 1995
Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene regionA A Bergen, J B ten Brink, F Riemslag, et al.
Genomics|April 1, 1993
Refinement of the localization of the X-linked ocular albinism geneA A Bergen, P Zijp, E J Schuurman, et al.
Genomics|November 1, 1993
Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3A A Bergen, F Meire, J ten Brink, et al.
Journal of Medical Genetics|October 1, 1996
Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1A A Bergen, J B ten Brink, F Riemslag, et al.
Ophthalmic Genetics|June 1, 1995
Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa familiesA A Bergen, L I Van den Born, E J Schuurman, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloningA A Bergen, M C Wapenaar, E J Schuurman, et al.
Human Genetics|December 1, 1991
Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls typeA A Bergen, C Samanns, E J Schuurman, et al.
Clinical Genetics|March 1, 1992
Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysisA A Bergen, E J Schuurman, L I van den Born, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Clinical Genetics|May 1, 1994
DNA carrier detection in X-linked progressive cone dystrophyA A Bergen, F Meire, E J Schuurman, et al.
Genomics|May 1, 1994
Nance-Horan syndrome: linkage analysis in a family from The NetherlandsA A Bergen, J ten Brink, E J Schuurman, et al.
Human Molecular Genetics|May 1, 1995
Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene regionA A Bergen, J B ten Brink, F Riemslag, et al.
Genomics|April 1, 1993
Refinement of the localization of the X-linked ocular albinism geneA A Bergen, P Zijp, E J Schuurman, et al.
Genomics|November 1, 1993
Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3A A Bergen, F Meire, J ten Brink, et al.
Journal of Medical Genetics|October 1, 1996
Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1A A Bergen, J B ten Brink, F Riemslag, et al.
Ophthalmic Genetics|June 1, 1995
Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa familiesA A Bergen, L I Van den Born, E J Schuurman, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloningA A Bergen, M C Wapenaar, E J Schuurman, et al.
Human Genetics|December 1, 1991
Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls typeA A Bergen, C Samanns, E J Schuurman, et al.
Clinical Genetics|March 1, 1992
Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysisA A Bergen, E J Schuurman, L I van den Born, et al.
Pageof 2