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

M Bobrow

Showing results (221-230 of 235) with videos related to

Pageof 24
Sort By:
Transplantation Proceedings|January 1, 1998
Evaluation of mitochondrial function after cold preservation of pancreatic islet cells from donors treated with pefloxacinJ Puc, P Kwiatkowski, M Bobrow, et al.
Journal of Medical Genetics|June 1, 1993
Further investigation of the HEXA gene intron 9 donor splice site mutation frequently found in non-Jewish Tay-Sachs disease patients from the British IslesE C Landels, P M Green, I H Ellis, et al.
BMJ (Clinical Research Ed.)|January 5, 2001
Raising concerns about family history of breast cancer in primary care consultations: prospective, population based study. Women's Concerns Study GroupF Hyland, A L Kinmonth, T M Marteau, et al.
Genomics|July 1, 1991
242 breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spreadL A Blonden, P M Grootscholten, J T den Dunnen, et al.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Lancet (London, England)|June 21, 1980
Early antenatal diagnosis of exomphalosN J Wald, H S Cuckle, R D Barlow, et al.
Annals of Human Genetics|January 1, 1980
Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16S Povey, S J Jeremiah, R F Barker, et al.
Genomics|February 1, 1988
A deletion hot spot in the Duchenne muscular dystrophy geneM C Wapenaar, T Kievits, K A Hart, et al.
Journal of Medical Genetics|October 4, 2005
Prenatal detection of unbalanced chromosomal rearrangements by array CGHL Rickman, H Fiegler, C Shaw-Smith, et al.
British Journal of Obstetrics and Gynaecology|February 1, 1979
Antenatal screening in Oxford for fetal neural tube defectsN J Wald, H S Cuckle, J Boreham, et al.
Pageof 24

Showing results (221-230 of 235) with videos related to

Sort By:
Pageof 24
Transplantation Proceedings|January 1, 1998
Evaluation of mitochondrial function after cold preservation of pancreatic islet cells from donors treated with pefloxacinJ Puc, P Kwiatkowski, M Bobrow, et al.
Journal of Medical Genetics|June 1, 1993
Further investigation of the HEXA gene intron 9 donor splice site mutation frequently found in non-Jewish Tay-Sachs disease patients from the British IslesE C Landels, P M Green, I H Ellis, et al.
BMJ (Clinical Research Ed.)|January 5, 2001
Raising concerns about family history of breast cancer in primary care consultations: prospective, population based study. Women's Concerns Study GroupF Hyland, A L Kinmonth, T M Marteau, et al.
Genomics|July 1, 1991
242 breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spreadL A Blonden, P M Grootscholten, J T den Dunnen, et al.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Lancet (London, England)|June 21, 1980
Early antenatal diagnosis of exomphalosN J Wald, H S Cuckle, R D Barlow, et al.
Annals of Human Genetics|January 1, 1980
Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16S Povey, S J Jeremiah, R F Barker, et al.
Genomics|February 1, 1988
A deletion hot spot in the Duchenne muscular dystrophy geneM C Wapenaar, T Kievits, K A Hart, et al.
Journal of Medical Genetics|October 4, 2005
Prenatal detection of unbalanced chromosomal rearrangements by array CGHL Rickman, H Fiegler, C Shaw-Smith, et al.
British Journal of Obstetrics and Gynaecology|February 1, 1979
Antenatal screening in Oxford for fetal neural tube defectsN J Wald, H S Cuckle, J Boreham, et al.
Pageof 24