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L M Bleeker-Wagemakers

Showing results (1-10 of 9) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1986
Peters' anomaly and systemic defectsM J van Schooneveld, J W Delleman, F A Beemer, et al.
Human Genetics|January 19, 1978
Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndromeJ B Bijlsma, H F de France, L M Bleeker-Wagemakers, et al.
Journal of Medical Genetics|December 1, 1994
Refinement of the chromosomal position of the X linked juvenile retinoschisis geneA A Bergen, J B ten Brink, L M Bleeker-Wagemakers, et al.
Journal of Medical Genetics|January 1, 1990
Oculocerebrocutaneous syndromeL M Bleeker-Wagemakers, B C Hamel, R C Hennekam, et al.
Human Genetics|January 1, 1985
Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosomeL M Bleeker-Wagemakers, U Friedrich, A Gal, et al.
Human Genetics|March 1, 1989
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpA Gal, A Schinzel, U Orth, et al.
Genomics|August 1, 1994
Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease populationS van Soest, L I van den Born, A Gal, et al.
Genomics|November 1, 1992
Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosaL M Bleeker-Wagemakers, A Gal, R Kumar-Singh, et al.
Human Molecular Genetics|July 1, 1996
Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1R Roepman, G van Duijnhoven, T Rosenberg, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1986
Peters' anomaly and systemic defectsM J van Schooneveld, J W Delleman, F A Beemer, et al.
Human Genetics|January 19, 1978
Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndromeJ B Bijlsma, H F de France, L M Bleeker-Wagemakers, et al.
Journal of Medical Genetics|December 1, 1994
Refinement of the chromosomal position of the X linked juvenile retinoschisis geneA A Bergen, J B ten Brink, L M Bleeker-Wagemakers, et al.
Journal of Medical Genetics|January 1, 1990
Oculocerebrocutaneous syndromeL M Bleeker-Wagemakers, B C Hamel, R C Hennekam, et al.
Human Genetics|January 1, 1985
Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosomeL M Bleeker-Wagemakers, U Friedrich, A Gal, et al.
Human Genetics|March 1, 1989
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpA Gal, A Schinzel, U Orth, et al.
Genomics|August 1, 1994
Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease populationS van Soest, L I van den Born, A Gal, et al.
Genomics|November 1, 1992
Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosaL M Bleeker-Wagemakers, A Gal, R Kumar-Singh, et al.
Human Molecular Genetics|July 1, 1996
Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1R Roepman, G van Duijnhoven, T Rosenberg, et al.
Pageof 1