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 C Hamel

Showing results (21-30 of 129) with videos related to

Pageof 13
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1996
Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolismW Ruitenbeek, U Wendel, B C Hamel, et al.
Progress in Clinical and Biological Research|January 1, 1989
Nephropathy in hereditary osteo-onycho dysplasia (HOOD): variable expression or genetic heterogeneity?E J Lommen, B C Hamel, R L te Slaa
Clinical Dysmorphology|April 1, 1997
Heminasal aplasia: a case report and review of the literature of the last 25 yearsA A van Kempen, F A Nabben, B C Hamel
American Journal of Medical Genetics|December 1, 1994
Oculo-ectodermal syndrome: a new caseM E Evers, R H Dijkman-Neerincx, B C Hamel
American Journal of Medical Genetics|May 30, 1998
A large family with multiple epiphyseal dysplasia linked to COL9A2 geneJ B van Mourik, B C Hamel, E C Mariman
Nederlands Tijdschrift Voor Geneeskunde|September 21, 1996
[Fatal arrhythmia following administration of suxamethonium to a postpartum woman who subsequently was found to have dystrophia myotonica]H I Wildschut, S Verhoef, J L Schilder, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Characteristic facial dysmorphism, arachnodactyly and mental retardation: another caseG J Van Buggenhout, A C Akkermans-Scholten, B C Hamel
Human Molecular Genetics|August 1, 1992
Improving the polymorphism content of the 3' UTR of the human IGF2R geneF A Hol, M P Geurds, B C Hamel, et al.
Journal of Medical Genetics|October 10, 1997
Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia: Boucher-Neuhäuser syndromeP Rump, B C Hamel, A J Pinckers, et al.
American Journal of Medical Genetics|March 1, 1990
Acrocallosal syndromeH J Hendriks, H G Brunner, T A Haagen, et al.
Pageof 13

Showing results (21-30 of 129) with videos related to

Sort By:
Pageof 13
Journal of Inherited Metabolic Disease|January 1, 1996
Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolismW Ruitenbeek, U Wendel, B C Hamel, et al.
Progress in Clinical and Biological Research|January 1, 1989
Nephropathy in hereditary osteo-onycho dysplasia (HOOD): variable expression or genetic heterogeneity?E J Lommen, B C Hamel, R L te Slaa
Clinical Dysmorphology|April 1, 1997
Heminasal aplasia: a case report and review of the literature of the last 25 yearsA A van Kempen, F A Nabben, B C Hamel
American Journal of Medical Genetics|December 1, 1994
Oculo-ectodermal syndrome: a new caseM E Evers, R H Dijkman-Neerincx, B C Hamel
American Journal of Medical Genetics|May 30, 1998
A large family with multiple epiphyseal dysplasia linked to COL9A2 geneJ B van Mourik, B C Hamel, E C Mariman
Nederlands Tijdschrift Voor Geneeskunde|September 21, 1996
[Fatal arrhythmia following administration of suxamethonium to a postpartum woman who subsequently was found to have dystrophia myotonica]H I Wildschut, S Verhoef, J L Schilder, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Characteristic facial dysmorphism, arachnodactyly and mental retardation: another caseG J Van Buggenhout, A C Akkermans-Scholten, B C Hamel
Human Molecular Genetics|August 1, 1992
Improving the polymorphism content of the 3' UTR of the human IGF2R geneF A Hol, M P Geurds, B C Hamel, et al.
Journal of Medical Genetics|October 10, 1997
Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia: Boucher-Neuhäuser syndromeP Rump, B C Hamel, A J Pinckers, et al.
American Journal of Medical Genetics|March 1, 1990
Acrocallosal syndromeH J Hendriks, H G Brunner, T A Haagen, et al.
Pageof 13