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

L Arbour

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
Prenatal Diagnosis|March 26, 2005
Prenatally detected trisomy 20 mosaicismW P Robinson, B McGillivray, M E S Lewis, et al.
American Journal of Medical Genetics|March 17, 2001
Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13)E Rajcan-Separovic, W P Robinson, M Stephenson, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
Discordant measures of androgen-binding kinetics in two mutant androgen receptors causing mild or partial androgen insensitivity, respectivelyD L Shkolny, L K Beitel, J Ginsberg, et al.
Oncogene|June 26, 1997
The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor geneN Rahman, L Arbour, P Tonin, et al.
International Journal of Circumpolar Health|November 6, 2004
Heart defects and other malformations in the Inuit in Canada: a baseline studyL Arbour, C Gilpin, V Millor-Roy, et al.
Prenatal Diagnosis|May 10, 2002
Prenatal diagnosis of apparently isolated unilateral multicystic kidney: implications for counselling and managementG Aubertin, S Cripps, G Coleman, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 26, 2012
Silver-catalysed enantioselective addition of O-H and N-H bonds to allenes: a new model for stereoselectivity based on noncovalent interactionsJannine L Arbour, Henry S Rzepa, Julia Contreras-García, et al.
The Journal of Pediatrics|September 1, 1996
Glutathione deficiency as a complication of methylmalonic acidemia: response to high doses of ascorbateE Treacy, L Arbour, P Chessex, et al.
Nature Genetics|August 1, 1996
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21N Rahman, L Arbour, P Tonin, et al.
American Journal of Medical Genetics|May 14, 1999
Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defectsB Christensen, L Arbour, P Tran, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|March 26, 2005
Prenatally detected trisomy 20 mosaicismW P Robinson, B McGillivray, M E S Lewis, et al.
American Journal of Medical Genetics|March 17, 2001
Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13)E Rajcan-Separovic, W P Robinson, M Stephenson, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
Discordant measures of androgen-binding kinetics in two mutant androgen receptors causing mild or partial androgen insensitivity, respectivelyD L Shkolny, L K Beitel, J Ginsberg, et al.
Oncogene|June 26, 1997
The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor geneN Rahman, L Arbour, P Tonin, et al.
International Journal of Circumpolar Health|November 6, 2004
Heart defects and other malformations in the Inuit in Canada: a baseline studyL Arbour, C Gilpin, V Millor-Roy, et al.
Prenatal Diagnosis|May 10, 2002
Prenatal diagnosis of apparently isolated unilateral multicystic kidney: implications for counselling and managementG Aubertin, S Cripps, G Coleman, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 26, 2012
Silver-catalysed enantioselective addition of O-H and N-H bonds to allenes: a new model for stereoselectivity based on noncovalent interactionsJannine L Arbour, Henry S Rzepa, Julia Contreras-García, et al.
The Journal of Pediatrics|September 1, 1996
Glutathione deficiency as a complication of methylmalonic acidemia: response to high doses of ascorbateE Treacy, L Arbour, P Chessex, et al.
Nature Genetics|August 1, 1996
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21N Rahman, L Arbour, P Tonin, et al.
American Journal of Medical Genetics|May 14, 1999
Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defectsB Christensen, L Arbour, P Tran, et al.
Pageof 3