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F P Cremers

Showing results (41-50 of 80) with videos related to

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Genomics|March 21, 1998
Complete exon-intron structure of the retina-specific ATP binding transporter gene (ABCR) allows the identification of novel mutations underlying Stargardt diseaseS Gerber, J M Rozet, T J van de Pol, et al.
Human Molecular Genetics|November 1, 1995
A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 geneY J de Kok, G F Merkx, S M van der Maarel, et al.
European Journal of Cell Biology|January 1, 1985
Ultrastructural localization and characterization of proteoglycans in human lung alveoliT H van Kuppevelt, F P Cremers, J G Domen, et al.
Human Molecular Genetics|July 1, 1994
Cloning and characterization of the human choroideremia geneH van Bokhoven, J A van den Hurk, L Bogerd, et al.
Journal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.
Somatic Cell and Molecular Genetics|January 1, 1994
Radiation hybrids for the proximal long arm of the X chromosome and their use in the derivation of an ordered set of cosmid markers from a defined subregion in proximal Xq13.1D Röhme, T Sidén, S M van der Maarel, et al.
Human Genetics|November 1, 1990
Cloning of the breakpoints of a deletion associated with choroidermiaF P Cremers, F Brunsmann, W Berger, et al.
Human Molecular Genetics|July 1, 1996
Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1S M van der Maarel, I H Scholten, I Huber, et al.
American Journal of Medical Genetics|December 1, 1992
Prenatal exclusion of choroideremiaJ A van den Hurk, P M van Zandvoort, F Brunsmann, et al.
Human Molecular Genetics|June 1, 1996
Identification of a gene disrupted by a microdeletion in a patient with X-linked retinitis pigmentosa (XLRP)R Roepman, D Bauer, T Rosenberg, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Genomics|March 21, 1998
Complete exon-intron structure of the retina-specific ATP binding transporter gene (ABCR) allows the identification of novel mutations underlying Stargardt diseaseS Gerber, J M Rozet, T J van de Pol, et al.
Human Molecular Genetics|November 1, 1995
A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 geneY J de Kok, G F Merkx, S M van der Maarel, et al.
European Journal of Cell Biology|January 1, 1985
Ultrastructural localization and characterization of proteoglycans in human lung alveoliT H van Kuppevelt, F P Cremers, J G Domen, et al.
Human Molecular Genetics|July 1, 1994
Cloning and characterization of the human choroideremia geneH van Bokhoven, J A van den Hurk, L Bogerd, et al.
Journal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.
Somatic Cell and Molecular Genetics|January 1, 1994
Radiation hybrids for the proximal long arm of the X chromosome and their use in the derivation of an ordered set of cosmid markers from a defined subregion in proximal Xq13.1D Röhme, T Sidén, S M van der Maarel, et al.
Human Genetics|November 1, 1990
Cloning of the breakpoints of a deletion associated with choroidermiaF P Cremers, F Brunsmann, W Berger, et al.
Human Molecular Genetics|July 1, 1996
Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1S M van der Maarel, I H Scholten, I Huber, et al.
American Journal of Medical Genetics|December 1, 1992
Prenatal exclusion of choroideremiaJ A van den Hurk, P M van Zandvoort, F Brunsmann, et al.
Human Molecular Genetics|June 1, 1996
Identification of a gene disrupted by a microdeletion in a patient with X-linked retinitis pigmentosa (XLRP)R Roepman, D Bauer, T Rosenberg, et al.
Pageof 8