Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F P Cremers

Showing results (61-70 of 80) with videos related to

Pageof 8
Sort By:
Human Molecular Genetics|August 1, 1995
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3M Bitner-Glindzicz, P Turnpenny, P Höglund, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremiaF P Cremers, D J van de Pol, B Wieringa, et al.
American Journal of Human Genetics|July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, 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.
Human Genetics|November 1, 1992
Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosomeW Berger, A Meindl, B de Leeuw, et al.
Human Mutation|January 1, 1997
Molecular basis of choroideremia (CHM): mutations involving the Rab escort protein-1 (REP-1) geneJ A van den Hurk, M Schwartz, H van Bokhoven, et al.
Human Molecular Genetics|June 1, 1997
Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germlineJ A van den Hurk, W Hendriks, D J van de Pol, et al.
Nature Genetics|August 11, 1998
Positional cloning of the gene for X-linked retinitis pigmentosa 2U Schwahn, S Lenzner, J Dong, et al.
Human Molecular Genetics|April 18, 1998
Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCRF P Cremers, D J van de Pol, M van Driel, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 15, 2001
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCHS J Bom, E M De Leenheer, F X Lemaire, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|August 1, 1995
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3M Bitner-Glindzicz, P Turnpenny, P Höglund, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremiaF P Cremers, D J van de Pol, B Wieringa, et al.
American Journal of Human Genetics|July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, 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.
Human Genetics|November 1, 1992
Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosomeW Berger, A Meindl, B de Leeuw, et al.
Human Mutation|January 1, 1997
Molecular basis of choroideremia (CHM): mutations involving the Rab escort protein-1 (REP-1) geneJ A van den Hurk, M Schwartz, H van Bokhoven, et al.
Human Molecular Genetics|June 1, 1997
Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germlineJ A van den Hurk, W Hendriks, D J van de Pol, et al.
Nature Genetics|August 11, 1998
Positional cloning of the gene for X-linked retinitis pigmentosa 2U Schwahn, S Lenzner, J Dong, et al.
Human Molecular Genetics|April 18, 1998
Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCRF P Cremers, D J van de Pol, M van Driel, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 15, 2001
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCHS J Bom, E M De Leenheer, F X Lemaire, et al.
Pageof 8