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

B A van Oost

Showing results (51-60 of 107) with videos related to

Pageof 11
Sort By:
Behavior Genetics|June 27, 2006
Phenotyping of aggressive behavior in golden retriever dogs with a questionnaireL van den Berg, M B H Schilder, H de Vries, et al.
American Journal of Medical Genetics|April 1, 1992
Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting maleA P Smits, B A van Oost, A F de Haan, et al.
Human Genetics|March 1, 1993
X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorderD D de Vries, I J de Wijs, G Wolff, et al.
Genomics|October 1, 1989
A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19H G Brunner, H Smeets, H M Lambermon, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
Cloning of the canine gene encoding transcription factor Pit-1 and its exclusion as candidate gene in a canine model of pituitary dwarfismI S Lantinga-van Leeuwen, J A Mol, H S Kooistra, et al.
Human Genetics|August 1, 1995
Two novel missense mutations in the cystathionine beta-synthase gene in homocystinuric patientsL A Kluijtmans, H J Blom, G H Boers, et al.
Human Genetics|March 1, 1996
A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch familyE A Sistermans, I J de Wijs, R F de Coo, et al.
European Journal of Pediatrics|July 1, 1994
Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcificationsJ F Samson, P G Barth, J I de Vries, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Mutation detection in the aspartoacylase gene in 17 patients with Canavan disease: four new mutations in the non-Jewish populationE A Sistermans, R F de Coo, H M van Beerendonk, et al.
American Journal of Medical Genetics|February 1, 1991
Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28B A Oostra, D F Majoor-Krakauer, J O van Hemel, et al.
Pageof 11

Showing results (51-60 of 107) with videos related to

Sort By:
Pageof 11
Behavior Genetics|June 27, 2006
Phenotyping of aggressive behavior in golden retriever dogs with a questionnaireL van den Berg, M B H Schilder, H de Vries, et al.
American Journal of Medical Genetics|April 1, 1992
Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting maleA P Smits, B A van Oost, A F de Haan, et al.
Human Genetics|March 1, 1993
X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorderD D de Vries, I J de Wijs, G Wolff, et al.
Genomics|October 1, 1989
A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19H G Brunner, H Smeets, H M Lambermon, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
Cloning of the canine gene encoding transcription factor Pit-1 and its exclusion as candidate gene in a canine model of pituitary dwarfismI S Lantinga-van Leeuwen, J A Mol, H S Kooistra, et al.
Human Genetics|August 1, 1995
Two novel missense mutations in the cystathionine beta-synthase gene in homocystinuric patientsL A Kluijtmans, H J Blom, G H Boers, et al.
Human Genetics|March 1, 1996
A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch familyE A Sistermans, I J de Wijs, R F de Coo, et al.
European Journal of Pediatrics|July 1, 1994
Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcificationsJ F Samson, P G Barth, J I de Vries, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Mutation detection in the aspartoacylase gene in 17 patients with Canavan disease: four new mutations in the non-Jewish populationE A Sistermans, R F de Coo, H M van Beerendonk, et al.
American Journal of Medical Genetics|February 1, 1991
Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28B A Oostra, D F Majoor-Krakauer, J O van Hemel, et al.
Pageof 11