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

P S Gerald

Showing results (41-50 of 66) with videos related to

Pageof 7
Sort By:
Birth Defects Original Article Series|January 1, 1982
Hirschsprung disease in progeny of affected individuals: a case report and review of the literatureR Carmi, P Hawley, J W Wood, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Expression of GAPDH and TPI in dog-rodent hybridsG A Bruns, P Pierce, V M Regina, et al.
American Journal of Medical Genetics|January 1, 1984
An anthropometric study of males with the fragile-X syndromeD L Meryash, C E Cronk, B Sachs, et al.
Experimental Cell Research|May 1, 1976
Fluorescence analysis of late DNA replication in mouse metaphase chromosomes using BUdR and 33258 HoechstK Madan, J W Allen, P S Gerald, et al.
Pediatrics|November 1, 1980
Wilms tumor in five cousinsJ F Cordero, F P Li, L B Holmes, et al.
Blood|March 1, 1972
Congenital methemoglobinemia: the result of age-dependent decay of methemoglobin reductaseS A Feig, D G Nathan, P S Gerald, et al.
Experimental Cell Research|August 1, 1974
Lateral asymmetry in the fluorescence of human Y chromosomes stained with 33 258 HoechstS A Latt, R L Davidson, M S Lin, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Lysosomal beta-D-galactosidase in man-hamster somatic cell hybridsG A Bruns, A C Leary, V M Regina, et al.
Journal of Ultrastructure Research|October 1, 1980
Heterogeneity of ciliary morphology in the immotile-cilia syndrome in manE E Schneeberger, J McCormack, H J Issenberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1975
Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemiaS A Latt, G Stetten, L A Juergens, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Birth Defects Original Article Series|January 1, 1982
Hirschsprung disease in progeny of affected individuals: a case report and review of the literatureR Carmi, P Hawley, J W Wood, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Expression of GAPDH and TPI in dog-rodent hybridsG A Bruns, P Pierce, V M Regina, et al.
American Journal of Medical Genetics|January 1, 1984
An anthropometric study of males with the fragile-X syndromeD L Meryash, C E Cronk, B Sachs, et al.
Experimental Cell Research|May 1, 1976
Fluorescence analysis of late DNA replication in mouse metaphase chromosomes using BUdR and 33258 HoechstK Madan, J W Allen, P S Gerald, et al.
Pediatrics|November 1, 1980
Wilms tumor in five cousinsJ F Cordero, F P Li, L B Holmes, et al.
Blood|March 1, 1972
Congenital methemoglobinemia: the result of age-dependent decay of methemoglobin reductaseS A Feig, D G Nathan, P S Gerald, et al.
Experimental Cell Research|August 1, 1974
Lateral asymmetry in the fluorescence of human Y chromosomes stained with 33 258 HoechstS A Latt, R L Davidson, M S Lin, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Lysosomal beta-D-galactosidase in man-hamster somatic cell hybridsG A Bruns, A C Leary, V M Regina, et al.
Journal of Ultrastructure Research|October 1, 1980
Heterogeneity of ciliary morphology in the immotile-cilia syndrome in manE E Schneeberger, J McCormack, H J Issenberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1975
Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemiaS A Latt, G Stetten, L A Juergens, et al.
Pageof 7