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

J L Watt

Showing results (21-30 of 46) with videos related to

Pageof 5
Sort By:
Chest|January 1, 1992
Is an abbreviated bronchial challenge with histamine valid?L E Schmidt, P S Thorne, J L Watt, et al.
Journal of Medical Genetics|April 1, 1990
Terminal deletion (14)(q32.3): a new caseN Telford, D A Thomson, M J Griffiths, et al.
Cancer Genetics and Cytogenetics|May 1, 1985
Chromosome damage and sister chromatid exchanges in lymphocyte cultures from patients with two primary cancersT Brown, A A Dawson, I A McDonald, et al.
Journal of Medical Genetics|August 1, 1986
A paracentric inversion of 7q illustrating a possible interchromosomal effectJ L Watt, K Ward, D A Couzin, et al.
Cancer Genetics and Cytogenetics|February 1, 1986
Variation of SCE frequency in lymphocyte cultures from patients with Hodgkin's disease before, during, and after treatmentT Brown, A A Dawson, D J King, et al.
Acta Haematologica|January 1, 1979
Clonal evolution of marker chromosomes in a case of myelofibrosis with myeloid metaplasia and myeloblastic transformationB M Page, J L Watt, I N Reid, et al.
Journal of Medical Genetics|October 1, 1984
A familial insertion involving an active nucleolar organiser within chromosome 12J L Watt, D A Couzin, D J Lloyd, et al.
Journal of Medical Genetics|June 1, 1981
Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0)J L Watt, D A Couzin, A W Johnston, et al.
Journal of Medical Genetics|October 1, 1981
Diplospermy II indicated as the origin of a liveborn human triploid (69,XXX)B M Page, E B Robson, P J Cook, et al.
Cancer Genetics and Cytogenetics|September 1, 1982
An unusual karyotype in preleukemiaJ L Watt, R R Khaund, S G Allan, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Chest|January 1, 1992
Is an abbreviated bronchial challenge with histamine valid?L E Schmidt, P S Thorne, J L Watt, et al.
Journal of Medical Genetics|April 1, 1990
Terminal deletion (14)(q32.3): a new caseN Telford, D A Thomson, M J Griffiths, et al.
Cancer Genetics and Cytogenetics|May 1, 1985
Chromosome damage and sister chromatid exchanges in lymphocyte cultures from patients with two primary cancersT Brown, A A Dawson, I A McDonald, et al.
Journal of Medical Genetics|August 1, 1986
A paracentric inversion of 7q illustrating a possible interchromosomal effectJ L Watt, K Ward, D A Couzin, et al.
Cancer Genetics and Cytogenetics|February 1, 1986
Variation of SCE frequency in lymphocyte cultures from patients with Hodgkin's disease before, during, and after treatmentT Brown, A A Dawson, D J King, et al.
Acta Haematologica|January 1, 1979
Clonal evolution of marker chromosomes in a case of myelofibrosis with myeloid metaplasia and myeloblastic transformationB M Page, J L Watt, I N Reid, et al.
Journal of Medical Genetics|October 1, 1984
A familial insertion involving an active nucleolar organiser within chromosome 12J L Watt, D A Couzin, D J Lloyd, et al.
Journal of Medical Genetics|June 1, 1981
Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0)J L Watt, D A Couzin, A W Johnston, et al.
Journal of Medical Genetics|October 1, 1981
Diplospermy II indicated as the origin of a liveborn human triploid (69,XXX)B M Page, E B Robson, P J Cook, et al.
Cancer Genetics and Cytogenetics|September 1, 1982
An unusual karyotype in preleukemiaJ L Watt, R R Khaund, S G Allan, et al.
Pageof 5