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

Clinical genetics

Showing results (691-700 of 7,173) with videos related to

Pageof 718
Sort By:
Clinical Genetics|October 1, 1990
X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of XqM Schwartz, M Haim, D Skarsholm
Clinical Genetics|June 10, 2011
5-Oxoprolinase deficiency: report of the first human OPLAH mutationI A Almaghlouth, J Y Mohamed, M Al-Amoudi, et al.
Clinical Genetics|December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.
Clinical Genetics|April 1, 1990
A cost-benefit analysis of prenatal diagnosis by amniocentesis in DenmarkH Goldstein, J Philip
Clinical Genetics|January 11, 2011
Lysosomal multienzymatic complex-related diseases: a genetic study among Portuguese patientsM F Coutinho, L Lacerda, S Macedo-Ribeiro, et al.
Clinical Genetics|October 16, 2007
Crouzon with acanthosis nigricans. Further delineation of the syndromeL Arnaud-López, R Fragoso, J Mantilla-Capacho, et al.
Clinical Genetics|October 16, 2007
Formalin-fixed paraffin-embedded clinical tissues show spurious copy number changes in array-CGH profilesE A Mc Sherry, A Mc Goldrick, E W Kay, et al.
Clinical Genetics|November 17, 2007
Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12J Davidsson, A Collin, M Oreberg, et al.
Clinical Genetics|October 1, 1991
Apolipoprotein B polymorphism and altered apolipoprotein B concentrations in Congolese blacksH J Parra, F Martin, F Monard, et al.
Clinical Genetics|October 1, 1991
Tuberous sclerosis in a child with de novo translocation t(3;12) (p26.3;q23.3)R Fahsold, H D Rott, U Claussen, et al.
Pageof 718

Showing results (691-700 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|October 1, 1990
X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of XqM Schwartz, M Haim, D Skarsholm
Clinical Genetics|June 10, 2011
5-Oxoprolinase deficiency: report of the first human OPLAH mutationI A Almaghlouth, J Y Mohamed, M Al-Amoudi, et al.
Clinical Genetics|December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.
Clinical Genetics|April 1, 1990
A cost-benefit analysis of prenatal diagnosis by amniocentesis in DenmarkH Goldstein, J Philip
Clinical Genetics|January 11, 2011
Lysosomal multienzymatic complex-related diseases: a genetic study among Portuguese patientsM F Coutinho, L Lacerda, S Macedo-Ribeiro, et al.
Clinical Genetics|October 16, 2007
Crouzon with acanthosis nigricans. Further delineation of the syndromeL Arnaud-López, R Fragoso, J Mantilla-Capacho, et al.
Clinical Genetics|October 16, 2007
Formalin-fixed paraffin-embedded clinical tissues show spurious copy number changes in array-CGH profilesE A Mc Sherry, A Mc Goldrick, E W Kay, et al.
Clinical Genetics|November 17, 2007
Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12J Davidsson, A Collin, M Oreberg, et al.
Clinical Genetics|October 1, 1991
Apolipoprotein B polymorphism and altered apolipoprotein B concentrations in Congolese blacksH J Parra, F Martin, F Monard, et al.
Clinical Genetics|October 1, 1991
Tuberous sclerosis in a child with de novo translocation t(3;12) (p26.3;q23.3)R Fahsold, H D Rott, U Claussen, et al.
Pageof 718