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 (21-30 of 80) with videos related to

Pageof 8
Sort By:
Human Mutation|January 1, 1993
Identification of mutations in Danish choroideremia familiesM Schwartz, T Rosenberg, J A van den Hurk, et al.
Nucleic Acids Research|March 25, 1992
Three RFLPs for pZ11 (DXS540) in the choroideremia gene at Xq21.2C M Molloy, T J van de Pol, R M Brohet, et al.
Human Genetics|November 10, 2001
DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elementsR Kirschner, D Erturk, C Zeitz, et al.
Human Reproduction (Oxford, England)|October 21, 1999
Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease?Y M van Kasteren, R D Hundscheid, A P Smits, et al.
Human Genetics|August 1, 1992
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutationH Traupe, D Müller, D Atherton, et al.
Human Molecular Genetics|December 6, 2001
CRB1 has a cytoplasmic domain that is functionally conserved between human and DrosophilaA I den Hollander, K Johnson, Y J de Kok, et al.
Human Genetics|March 1, 1993
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphismH Traupe, U Vetter, R Happle, et al.
The British Journal of Ophthalmology|July 22, 1999
Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR geneB J Klevering, M van Driel, D J van de Pol, et al.
Clinical Genetics|December 1, 1987
Deletion of the DXS165 locus in patients with classical choroideremiaF P Cremers, F Brunsmann, T J van de Pol, et al.
Ophthalmic Genetics|September 1, 1996
A highly polymorphic microsatellite marker located within the choroideremia geneH Van Bokhoven, J A Van den Hurk, L Bogerd, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
Human Mutation|January 1, 1993
Identification of mutations in Danish choroideremia familiesM Schwartz, T Rosenberg, J A van den Hurk, et al.
Nucleic Acids Research|March 25, 1992
Three RFLPs for pZ11 (DXS540) in the choroideremia gene at Xq21.2C M Molloy, T J van de Pol, R M Brohet, et al.
Human Genetics|November 10, 2001
DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elementsR Kirschner, D Erturk, C Zeitz, et al.
Human Reproduction (Oxford, England)|October 21, 1999
Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease?Y M van Kasteren, R D Hundscheid, A P Smits, et al.
Human Genetics|August 1, 1992
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutationH Traupe, D Müller, D Atherton, et al.
Human Molecular Genetics|December 6, 2001
CRB1 has a cytoplasmic domain that is functionally conserved between human and DrosophilaA I den Hollander, K Johnson, Y J de Kok, et al.
Human Genetics|March 1, 1993
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphismH Traupe, U Vetter, R Happle, et al.
The British Journal of Ophthalmology|July 22, 1999
Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR geneB J Klevering, M van Driel, D J van de Pol, et al.
Clinical Genetics|December 1, 1987
Deletion of the DXS165 locus in patients with classical choroideremiaF P Cremers, F Brunsmann, T J van de Pol, et al.
Ophthalmic Genetics|September 1, 1996
A highly polymorphic microsatellite marker located within the choroideremia geneH Van Bokhoven, J A Van den Hurk, L Bogerd, et al.
Pageof 8