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

S A Berend

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

Pageof 1
Sort By:
Clinical Genetics|July 28, 1999
Pure trisomy 10p involving an isochromosome 10pS A Berend, L G Shaffer, B A Bejjani
American Journal of Human Genetics|April 25, 2000
Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomesS A Berend, J Horwitz, C McCaskill, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Cytogenetics of collared lemmings (Dicrostonyx groenlandicus). I. Meiotic behavior and evolution of the neo-XY sex-chromosome systemS A Berend, D W Hale, M D Engstrom, et al.
Cytogenetics and Cell Genetics|April 30, 2002
Cytogenetics of collared lemmings (Dicrostonyx groenlandicus). II. Meiotic behavior of B chromosomes suggests a Y-chromosome origin of supernumerary chromosomesS A Berend, D W Hale, M D Engstrom, et al.
American Journal of Medical Genetics|December 8, 1998
Molecular analysis of mosaicism for two different de novo acrocentric rearrangements demonstrates diversity in Robertsonian translocation formationS A Berend, S Canún, C McCaskill, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 2, 2001
Satellite III sequences on 14p and their relevance to Robertsonian translocation formationR Bandyopadhyay, S A Berend, S L Page, et al.
American Journal of Medical Genetics|April 5, 2000
Deletion (9) (p13.1 p21.1)F Scaglia, O A Bodamer, S A Berend, et al.
American Journal of Medical Genetics|April 24, 1999
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomyS A Berend, G L Feldman, C McCaskill, et al.
American Journal of Medical Genetics|April 15, 2000
Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II lociS A Berend, A S Spikes, C D Kashork, et al.
Clinical Genetics|March 21, 2002
Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derived from chromosome 17: molecular analysis and delineation of the phenotypeP Stankiewicz, S S Parka, S E Holder, et al.
Pageof 1

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

Sort By:
Pageof 1
Clinical Genetics|July 28, 1999
Pure trisomy 10p involving an isochromosome 10pS A Berend, L G Shaffer, B A Bejjani
American Journal of Human Genetics|April 25, 2000
Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomesS A Berend, J Horwitz, C McCaskill, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Cytogenetics of collared lemmings (Dicrostonyx groenlandicus). I. Meiotic behavior and evolution of the neo-XY sex-chromosome systemS A Berend, D W Hale, M D Engstrom, et al.
Cytogenetics and Cell Genetics|April 30, 2002
Cytogenetics of collared lemmings (Dicrostonyx groenlandicus). II. Meiotic behavior of B chromosomes suggests a Y-chromosome origin of supernumerary chromosomesS A Berend, D W Hale, M D Engstrom, et al.
American Journal of Medical Genetics|December 8, 1998
Molecular analysis of mosaicism for two different de novo acrocentric rearrangements demonstrates diversity in Robertsonian translocation formationS A Berend, S Canún, C McCaskill, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 2, 2001
Satellite III sequences on 14p and their relevance to Robertsonian translocation formationR Bandyopadhyay, S A Berend, S L Page, et al.
American Journal of Medical Genetics|April 5, 2000
Deletion (9) (p13.1 p21.1)F Scaglia, O A Bodamer, S A Berend, et al.
American Journal of Medical Genetics|April 24, 1999
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomyS A Berend, G L Feldman, C McCaskill, et al.
American Journal of Medical Genetics|April 15, 2000
Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II lociS A Berend, A S Spikes, C D Kashork, et al.
Clinical Genetics|March 21, 2002
Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derived from chromosome 17: molecular analysis and delineation of the phenotypeP Stankiewicz, S S Parka, S E Holder, et al.
Pageof 1