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 P Lazarou

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
Nucleic Acids Research|June 10, 1988
RFLP for the human erb-A beta locusF S Wyllie, L P Lazarou, D Wynford-Thomas
Kidney International|July 20, 1999
Familial phenotype differences in PKD11N Hateboer, L P Lazarou, A J Williams, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 31, 2000
Co-occurrence of autosomal dominant polycystic kidney disease and Marfan syndrome in a kindredN Hateboer, M Buchalter, S J Davies, et al.
Journal of Medical Genetics|August 1, 1987
Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales populationL P Lazarou, F Davies, M Sarfarazi, et al.
Journal of Medical Genetics|August 1, 1990
Exclusion testing in pregnancy for Huntington's diseaseA Tyler, O W Quarrell, L P Lazarou, et al.
Journal of the Neurological Sciences|August 1, 1993
Immunohistological evidence for second or somatic mutations as the underlying cause of dystrophin expression by isolated fibres in Xp21 muscular dystrophy of Duchenne-type severityC Wallgren-Pettersson, B Jasani, L G Rosser, et al.
American Journal of Medical Genetics|August 1, 1992
Five years experience of predictive testing for myotonic dystrophy using linked DNA markersW Reardon, J L Floyd, J Myring, et al.
Journal of Medical Genetics|February 21, 2008
High frequency of genomic deletions--and a duplication--in the LIS1 gene in lissencephaly: implications for molecular diagnosisD Mei, R Lewis, E Parrini, et al.
Nucleic Acids Research|October 11, 1991
MboI RFLP at the D4S43 (C4H) locusL P Lazarou, R G Snell, M E MacDonald, et al.
Clinical Genetics|March 1, 1993
Huntington's disease: predictive testing and the molecular genetics laboratoryL P Lazarou, A L Meredith, J M Myring, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|June 10, 1988
RFLP for the human erb-A beta locusF S Wyllie, L P Lazarou, D Wynford-Thomas
Kidney International|July 20, 1999
Familial phenotype differences in PKD11N Hateboer, L P Lazarou, A J Williams, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 31, 2000
Co-occurrence of autosomal dominant polycystic kidney disease and Marfan syndrome in a kindredN Hateboer, M Buchalter, S J Davies, et al.
Journal of Medical Genetics|August 1, 1987
Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales populationL P Lazarou, F Davies, M Sarfarazi, et al.
Journal of Medical Genetics|August 1, 1990
Exclusion testing in pregnancy for Huntington's diseaseA Tyler, O W Quarrell, L P Lazarou, et al.
Journal of the Neurological Sciences|August 1, 1993
Immunohistological evidence for second or somatic mutations as the underlying cause of dystrophin expression by isolated fibres in Xp21 muscular dystrophy of Duchenne-type severityC Wallgren-Pettersson, B Jasani, L G Rosser, et al.
American Journal of Medical Genetics|August 1, 1992
Five years experience of predictive testing for myotonic dystrophy using linked DNA markersW Reardon, J L Floyd, J Myring, et al.
Journal of Medical Genetics|February 21, 2008
High frequency of genomic deletions--and a duplication--in the LIS1 gene in lissencephaly: implications for molecular diagnosisD Mei, R Lewis, E Parrini, et al.
Nucleic Acids Research|October 11, 1991
MboI RFLP at the D4S43 (C4H) locusL P Lazarou, R G Snell, M E MacDonald, et al.
Clinical Genetics|March 1, 1993
Huntington's disease: predictive testing and the molecular genetics laboratoryL P Lazarou, A L Meredith, J M Myring, et al.
Pageof 2