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 (1-10 of 80) with videos related to

Pageof 8
Sort By:
Current Opinion in Neurology|March 4, 1998
Genetic causes of hearing lossF P Cremers
Advances in Oto-Rhino-Laryngology|June 27, 2000
The ins and outs of X-linked deafness type 3F P Cremers, C W Cremers, H H Ropers
Human Molecular Genetics|August 1, 1994
Dinucleotide repeat polymorphism within the choroideremia gene at Xq21.2H van Bokhoven, C van Genderen, H H Ropers, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Assignment1 of H7365 (C9orf2) to human chromosome band 9q31 by somatic cell hybrid analysis and fluorescence in situ hybridizationD W Eib, G F Merkx, G J Martens, et al.
Human Genetics|August 1, 1992
Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21I Bach, D Robinson, N Thomas, et al.
Current Opinion in Genetics & Development|June 1, 1995
Mapping and cloning hereditary deafness genesF P Cremers, M Bitner-Glindzicz, M E Pembrey, et al.
The Histochemical Journal|June 1, 1984
Staining of proteoglycans in mouse lung alveoli. II. Characterization of the Cuprolinic blue-positive, anionic sitesT H van Kuppevelt, F P Cremers, J G Domen, et al.
The Histochemical Journal|June 1, 1984
Staining of proteoglycans in mouse lung alveoli. I. Ultrastructural localization of anionic sitesT H Van Kuppevelt, J G Domen, F P Cremers, et al.
Gene|January 1, 1985
Two human gamma-crystallin genes are linked and riddled with Alu-repeatsJ T den Dunnen, R J Moormann, F P Cremers, et al.
Human Mutation|January 1, 1997
The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutationY J de Kok, C W Cremers, H H Ropers, et al.
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Current Opinion in Neurology|March 4, 1998
Genetic causes of hearing lossF P Cremers
Advances in Oto-Rhino-Laryngology|June 27, 2000
The ins and outs of X-linked deafness type 3F P Cremers, C W Cremers, H H Ropers
Human Molecular Genetics|August 1, 1994
Dinucleotide repeat polymorphism within the choroideremia gene at Xq21.2H van Bokhoven, C van Genderen, H H Ropers, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Assignment1 of H7365 (C9orf2) to human chromosome band 9q31 by somatic cell hybrid analysis and fluorescence in situ hybridizationD W Eib, G F Merkx, G J Martens, et al.
Human Genetics|August 1, 1992
Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21I Bach, D Robinson, N Thomas, et al.
Current Opinion in Genetics & Development|June 1, 1995
Mapping and cloning hereditary deafness genesF P Cremers, M Bitner-Glindzicz, M E Pembrey, et al.
The Histochemical Journal|June 1, 1984
Staining of proteoglycans in mouse lung alveoli. II. Characterization of the Cuprolinic blue-positive, anionic sitesT H van Kuppevelt, F P Cremers, J G Domen, et al.
The Histochemical Journal|June 1, 1984
Staining of proteoglycans in mouse lung alveoli. I. Ultrastructural localization of anionic sitesT H Van Kuppevelt, J G Domen, F P Cremers, et al.
Gene|January 1, 1985
Two human gamma-crystallin genes are linked and riddled with Alu-repeatsJ T den Dunnen, R J Moormann, F P Cremers, et al.
Human Mutation|January 1, 1997
The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutationY J de Kok, C W Cremers, H H Ropers, et al.
Pageof 8