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

K F Kelly

Showing results (11-20 of 29) with videos related to

Pageof 3
Sort By:
Journal of Medical Genetics|July 1, 1994
Evaluation of laboratory methods for cystic fibrosis carrier screening: reliability, sensitivity, specificity, and costsZ H Miedzybrodzka, Z Yin, K F Kelly, et al.
Clinical and Laboratory Haematology|January 26, 2000
Thrombosis, markers of thrombotic risk, indwelling central venous catheters and antithrombotic prophylaxis using low-dose warfarin in subjects with malignant diseaseM Ratcliffe, C Broadfoot, M Davidson, et al.
BMJ (Clinical Research Ed.)|January 5, 1991
Screening for carriers of cystic fibrosisJ C Dean, K F Kelly, Z Miedzybrodzka, et al.
Clinical Genetics|June 1, 1989
Linkage in a family with X-linked Charcot-Marie-Tooth diseaseN Haites, N Fairweather, C Clark, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
From the cover: nanoscale imaging of chemical interactions: fluorine on graphiteK F Kelly, E T Mickelson, R H Hauge, et al.
Molecular and Cellular Endocrinology|October 1, 1988
Effects of oestrogen on the expression of a 4.4 kb mRNA in the ZR-75-1 human breast cancer cell lineD L Manning, R J Daly, P G Lord, et al.
Cancer Chemotherapy and Pharmacology|January 1, 1988
In vitro antiproliferative activity of 2'-(2-hydroxyphenyl)-2'-thiazoline-4'-carboxylic acid and its methyl ester on L1210 and P388 murine neoplasmsG T Elliot, K F Kelly, R L Bonna, et al.
Journal of Medical Genetics|July 29, 1999
Fragile X syndrome with FMR1 and FMR2 deletionS J Moore, L Strain, G F Cole, et al.
Journal of Medical Genetics|September 1, 1992
Autosomal dominant retinitis pigmentosa (ADRP): a rhodopsin mutation in a Scottish familyC Bell, C A Converse, M F Collins, et al.
Prenatal Diagnosis|July 1, 1991
Prenatal diagnosis for dystrophia myotonica using the polymerase chain reactionC Clark, K F Kelly, N Smith, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|July 1, 1994
Evaluation of laboratory methods for cystic fibrosis carrier screening: reliability, sensitivity, specificity, and costsZ H Miedzybrodzka, Z Yin, K F Kelly, et al.
Clinical and Laboratory Haematology|January 26, 2000
Thrombosis, markers of thrombotic risk, indwelling central venous catheters and antithrombotic prophylaxis using low-dose warfarin in subjects with malignant diseaseM Ratcliffe, C Broadfoot, M Davidson, et al.
BMJ (Clinical Research Ed.)|January 5, 1991
Screening for carriers of cystic fibrosisJ C Dean, K F Kelly, Z Miedzybrodzka, et al.
Clinical Genetics|June 1, 1989
Linkage in a family with X-linked Charcot-Marie-Tooth diseaseN Haites, N Fairweather, C Clark, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
From the cover: nanoscale imaging of chemical interactions: fluorine on graphiteK F Kelly, E T Mickelson, R H Hauge, et al.
Molecular and Cellular Endocrinology|October 1, 1988
Effects of oestrogen on the expression of a 4.4 kb mRNA in the ZR-75-1 human breast cancer cell lineD L Manning, R J Daly, P G Lord, et al.
Cancer Chemotherapy and Pharmacology|January 1, 1988
In vitro antiproliferative activity of 2'-(2-hydroxyphenyl)-2'-thiazoline-4'-carboxylic acid and its methyl ester on L1210 and P388 murine neoplasmsG T Elliot, K F Kelly, R L Bonna, et al.
Journal of Medical Genetics|July 29, 1999
Fragile X syndrome with FMR1 and FMR2 deletionS J Moore, L Strain, G F Cole, et al.
Journal of Medical Genetics|September 1, 1992
Autosomal dominant retinitis pigmentosa (ADRP): a rhodopsin mutation in a Scottish familyC Bell, C A Converse, M F Collins, et al.
Prenatal Diagnosis|July 1, 1991
Prenatal diagnosis for dystrophia myotonica using the polymerase chain reactionC Clark, K F Kelly, N Smith, et al.
Pageof 3