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 M Connor

Showing results (141-150 of 181) with videos related to

Pageof 19
Sort By:
Prenatal Diagnosis|August 19, 1999
Second-trimester pregnancy associated plasma protein-A levels are reduced in Cornelia de Lange syndrome pregnanciesD A Aitken, M Ireland, E Berry, et al.
Prenatal Diagnosis|August 1, 1993
First-trimester biochemical screening for fetal chromosome abnormalities and neural tube defectsD A Aitken, G McCaw, J A Crossley, et al.
Journal of Medical Genetics|August 1, 1989
Evidence for genetic heterogeneity in tuberous sclerosisJ R Sampson, J R Yates, L A Pirrit, et al.
Journal of Medical Genetics|December 1, 1985
Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of ScotlandJ M Connor, A F Pettigrew, I M Hann, et al.
Journal of Medical Genetics|January 1, 1987
Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditionsJ M Connor, L A Pirrit, J R Yates, et al.
Physiological Research|February 15, 2007
Demystification of Chester porphyria: a nonsense mutation in the Porphobilinogen Deaminase geneP Poblete-Gutiérrez, T Wiederholt, A Martinez-Mir, et al.
Journal of Surgical Oncology|October 1, 1995
Expression and loss of heterozygosity of c-met proto-oncogene in primary breast cancerJ Nagy, J S Clark, A Cooke, et al.
Molecular and Cellular Probes|August 1, 1997
Acute intermittent porphyria: the in vitro expression of mutant hydroxymethylbilane synthaseP M Ong, W G Lanyon, G Graham, et al.
Human Heredity|February 17, 1998
Identification of two novel mutations in the hydroxymethylbilane synthase gene in three patients from two unrelated families with acute intermittent porphyriaP M Ong, W G Lanyon, R J Hift, et al.
Molecular and Cellular Probes|February 1, 1996
Detection of four mutations in six unrelated South African patients with acute intermittent porphyriaP M Ong, W G Lanyon, R J Hift, et al.
Pageof 19

Showing results (141-150 of 181) with videos related to

Sort By:
Pageof 19
Prenatal Diagnosis|August 19, 1999
Second-trimester pregnancy associated plasma protein-A levels are reduced in Cornelia de Lange syndrome pregnanciesD A Aitken, M Ireland, E Berry, et al.
Prenatal Diagnosis|August 1, 1993
First-trimester biochemical screening for fetal chromosome abnormalities and neural tube defectsD A Aitken, G McCaw, J A Crossley, et al.
Journal of Medical Genetics|August 1, 1989
Evidence for genetic heterogeneity in tuberous sclerosisJ R Sampson, J R Yates, L A Pirrit, et al.
Journal of Medical Genetics|December 1, 1985
Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of ScotlandJ M Connor, A F Pettigrew, I M Hann, et al.
Journal of Medical Genetics|January 1, 1987
Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditionsJ M Connor, L A Pirrit, J R Yates, et al.
Physiological Research|February 15, 2007
Demystification of Chester porphyria: a nonsense mutation in the Porphobilinogen Deaminase geneP Poblete-Gutiérrez, T Wiederholt, A Martinez-Mir, et al.
Journal of Surgical Oncology|October 1, 1995
Expression and loss of heterozygosity of c-met proto-oncogene in primary breast cancerJ Nagy, J S Clark, A Cooke, et al.
Molecular and Cellular Probes|August 1, 1997
Acute intermittent porphyria: the in vitro expression of mutant hydroxymethylbilane synthaseP M Ong, W G Lanyon, G Graham, et al.
Human Heredity|February 17, 1998
Identification of two novel mutations in the hydroxymethylbilane synthase gene in three patients from two unrelated families with acute intermittent porphyriaP M Ong, W G Lanyon, R J Hift, et al.
Molecular and Cellular Probes|February 1, 1996
Detection of four mutations in six unrelated South African patients with acute intermittent porphyriaP M Ong, W G Lanyon, R J Hift, et al.
Pageof 19