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F P Cremers

Showing results (51-60 of 80) with videos related to

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Nature Genetics|September 1, 1992
Isolation of a candidate gene for Norrie disease by positional cloningW Berger, A Meindl, T J van de Pol, et al.
Nature Genetics|June 1, 1992
Isolation of a candidate gene for Norrie disease by positional cloningW Berger, A Meindl, T J van de Pol, et al.
American Journal of Human Genetics|October 1, 1988
Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqF P Cremers, T J van de Pol, B Wieringa, et al.
Human Molecular Genetics|May 1, 1992
An autosomal homologue of the choroideremia gene colocalizes with the Usher syndrome type II locus on the distal part of chromosome 1qF P Cremers, C M Molloy, D J van de Pol, et al.
American Journal of Human Genetics|October 1, 1990
Deletions in patients with classical choroideremia vary in size from 45 kb to several megabasesF P Cremers, E M Sankila, F Brunsmann, et al.
Neurology|January 1, 1993
Kearns-Sayre syndrome with a phenocopy of choroideremia instead of pigmentary retinopathyN H Herzberg, M J van Schooneveld, E M Bleeker-Wagemakers, et al.
Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.
Genomics|June 10, 1995
A high-resolution interval map of the q21 region of the human X chromosomeC Philippe, C Arnould, F Sloan, et al.
Human Mutation|April 24, 2001
Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness familiesZ H Shah, M Toompuu, T Hakkinen, et al.
Genomics|June 22, 1999
Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
Nature Genetics|September 1, 1992
Isolation of a candidate gene for Norrie disease by positional cloningW Berger, A Meindl, T J van de Pol, et al.
Nature Genetics|June 1, 1992
Isolation of a candidate gene for Norrie disease by positional cloningW Berger, A Meindl, T J van de Pol, et al.
American Journal of Human Genetics|October 1, 1988
Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqF P Cremers, T J van de Pol, B Wieringa, et al.
Human Molecular Genetics|May 1, 1992
An autosomal homologue of the choroideremia gene colocalizes with the Usher syndrome type II locus on the distal part of chromosome 1qF P Cremers, C M Molloy, D J van de Pol, et al.
American Journal of Human Genetics|October 1, 1990
Deletions in patients with classical choroideremia vary in size from 45 kb to several megabasesF P Cremers, E M Sankila, F Brunsmann, et al.
Neurology|January 1, 1993
Kearns-Sayre syndrome with a phenocopy of choroideremia instead of pigmentary retinopathyN H Herzberg, M J van Schooneveld, E M Bleeker-Wagemakers, et al.
Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.
Genomics|June 10, 1995
A high-resolution interval map of the q21 region of the human X chromosomeC Philippe, C Arnould, F Sloan, et al.
Human Mutation|April 24, 2001
Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness familiesZ H Shah, M Toompuu, T Hakkinen, et al.
Genomics|June 22, 1999
Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.
Pageof 8