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 L Pearson

Showing results (41-50 of 211) with videos related to

Pageof 22
Sort By:
Brain Research. Developmental Brain Research|January 22, 1996
The prepubertal ontogeny of neuropeptide Y-like immunoreactivity in the male Meishan pig brainP L Pearson, L L Anderson, C D Jacobson
Cytogenetics and Cell Genetics|January 1, 1987
Report of the committee on human gene mapping by recombinant DNA techniquesP L Pearson, K K Kidd, H F Willard
Nucleic Acids Research|January 25, 1990
P9 (DXYS75) detects a VNTR-type RFLP in the pseudoautosomal regionM C Wapenaar, P L Pearson, G J van Ommen
Cytogenetics and Cell Genetics|January 1, 1974
Proceedings: Localization of gene markers to regions of the human X chromosome by segregation of X-autosome translocations in somatic cell hybridsP L Pearson, A G van der Linden, A Hagemeijer
Nucleic Acids Research|March 11, 1986
Sequence heterogeneity within the human alphoid repetitive DNA familyP Devilee, P Slagboom, C J Cornelisse, et al.
Cytogenetics and Cell Genetics|January 1, 1975
Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocationJ De Wit, D Bootsma, P L Pearson, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Regional localization of the genes coding for human red cell adenylate kinase, aconitase, and galactose-1-phosphate uridylyltransferase on chromosome 9A Westerveld, J Garver, M A Nijman, et al.
Genomics|August 1, 1993
Isolation and characterization of an ornithine aminotransferase-related sequence (OATL3) mapping to 10q26M T Geraghty, W G Kearns, P L Pearson, et al.
Nature|June 4, 1971
Quinacrine fluorescence in mammalian chromosomesP L Pearson, M Bobrow, C G Vosa, et al.
Journal of Medical Genetics|January 1, 1987
The fragile X syndrome in a large family. I. Cytogenetic and clinical investigationsH Veenema, J P Geraedts, G C Beverstock, et al.
Pageof 22

Showing results (41-50 of 211) with videos related to

Sort By:
Pageof 22
Brain Research. Developmental Brain Research|January 22, 1996
The prepubertal ontogeny of neuropeptide Y-like immunoreactivity in the male Meishan pig brainP L Pearson, L L Anderson, C D Jacobson
Cytogenetics and Cell Genetics|January 1, 1987
Report of the committee on human gene mapping by recombinant DNA techniquesP L Pearson, K K Kidd, H F Willard
Nucleic Acids Research|January 25, 1990
P9 (DXYS75) detects a VNTR-type RFLP in the pseudoautosomal regionM C Wapenaar, P L Pearson, G J van Ommen
Cytogenetics and Cell Genetics|January 1, 1974
Proceedings: Localization of gene markers to regions of the human X chromosome by segregation of X-autosome translocations in somatic cell hybridsP L Pearson, A G van der Linden, A Hagemeijer
Nucleic Acids Research|March 11, 1986
Sequence heterogeneity within the human alphoid repetitive DNA familyP Devilee, P Slagboom, C J Cornelisse, et al.
Cytogenetics and Cell Genetics|January 1, 1975
Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocationJ De Wit, D Bootsma, P L Pearson, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Regional localization of the genes coding for human red cell adenylate kinase, aconitase, and galactose-1-phosphate uridylyltransferase on chromosome 9A Westerveld, J Garver, M A Nijman, et al.
Genomics|August 1, 1993
Isolation and characterization of an ornithine aminotransferase-related sequence (OATL3) mapping to 10q26M T Geraghty, W G Kearns, P L Pearson, et al.
Nature|June 4, 1971
Quinacrine fluorescence in mammalian chromosomesP L Pearson, M Bobrow, C G Vosa, et al.
Journal of Medical Genetics|January 1, 1987
The fragile X syndrome in a large family. I. Cytogenetic and clinical investigationsH Veenema, J P Geraedts, G C Beverstock, et al.
Pageof 22