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

M Caggana

Showing results (11-20 of 28) with videos related to

Pageof 3
Sort By:
Molecular Genetics and Metabolism|March 29, 2011
Newborn screening for Tyr-I: two years' experience of the New York State programM A Morrissey, S Sunny, A Fahim, et al.
Annals of Human Genetics|January 25, 2002
Estimate of the frequency of Wilson's disease in the US Caucasian population: a mutation analysis approachL Olivarez, M Caggana, K A Pass, et al.
American Journal of Medical Genetics|December 11, 1996
Prenatal diagnosis of a fetus with two balanced de novo chromosome rearrangementsP D Cotter, M Caggana, J P Willner, et al.
Environmental and Molecular Mutagenesis|January 1, 1991
In vivo somatic mutation in the lymphocytes of Hodgkin's disease patientsM Caggana, H L Liber, P M Mauch, et al.
Mutagenesis|September 1, 1991
Single-strand conformation polymorphisms can be used to detect T cell receptor gene rearrangements: an application to the in vivo hprt mutation assayM Caggana, M B Benjamin, J B Little, et al.
Clinical Genetics|March 18, 2004
The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defectsT Fitzgerald, S Duva, H Ostrer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Population-based studies reveal differences in the allelic frequencies of two functionally significant human interleukin-4 receptor polymorphisms in several ethnic groupsM Caggana, K Walker, A A Reilly, et al.
Mutation Research|December 1, 1991
In vivo exposure of human lymphocytes to technetium-99m in nuclear medicine patients does not induce detectable genetic effectsK T Kelsey, K J Donohoe, A Memisoglu, et al.
Annales De Genetique|January 1, 1997
Homozygosity for pericentric inversions of chromosome 9. Prenatal diagnosis of two casesP D Cotter, A Babu, L D McCurdy, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 1, 1992
A prospective study of hprt mutant and mutation frequencies in treated cancer patientsM Caggana, H L Liber, C N Coleman, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Molecular Genetics and Metabolism|March 29, 2011
Newborn screening for Tyr-I: two years' experience of the New York State programM A Morrissey, S Sunny, A Fahim, et al.
Annals of Human Genetics|January 25, 2002
Estimate of the frequency of Wilson's disease in the US Caucasian population: a mutation analysis approachL Olivarez, M Caggana, K A Pass, et al.
American Journal of Medical Genetics|December 11, 1996
Prenatal diagnosis of a fetus with two balanced de novo chromosome rearrangementsP D Cotter, M Caggana, J P Willner, et al.
Environmental and Molecular Mutagenesis|January 1, 1991
In vivo somatic mutation in the lymphocytes of Hodgkin's disease patientsM Caggana, H L Liber, P M Mauch, et al.
Mutagenesis|September 1, 1991
Single-strand conformation polymorphisms can be used to detect T cell receptor gene rearrangements: an application to the in vivo hprt mutation assayM Caggana, M B Benjamin, J B Little, et al.
Clinical Genetics|March 18, 2004
The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defectsT Fitzgerald, S Duva, H Ostrer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Population-based studies reveal differences in the allelic frequencies of two functionally significant human interleukin-4 receptor polymorphisms in several ethnic groupsM Caggana, K Walker, A A Reilly, et al.
Mutation Research|December 1, 1991
In vivo exposure of human lymphocytes to technetium-99m in nuclear medicine patients does not induce detectable genetic effectsK T Kelsey, K J Donohoe, A Memisoglu, et al.
Annales De Genetique|January 1, 1997
Homozygosity for pericentric inversions of chromosome 9. Prenatal diagnosis of two casesP D Cotter, A Babu, L D McCurdy, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 1, 1992
A prospective study of hprt mutant and mutation frequencies in treated cancer patientsM Caggana, H L Liber, C N Coleman, et al.
Pageof 3