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 Hamabe

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

Pageof 1
Sort By:
Nucleic Acids Research|September 25, 1990
StyI polymorphism at the D15S11 locusJ Hamabe, N Niikawa
Nucleic Acids Research|August 25, 1991
A DraI RFLP detected for probe pIR4-3R [D15S11] on chromosome 15qJ Hamabe, N Niikawa
Nucleic Acids Research|September 11, 1991
A BsaBI RFLP detected for probe pML34 [D15S9] on chromosome 15qJ Hamabe, S Saitoh, N Niikawa
Nucleic Acids Research|August 25, 1991
An ApaI RFLP for the human porphobilinogen deaminase gene (PBGD)J Hamabe, H Irifune, N Niikawa
Clinical Genetics|December 1, 1990
Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locusI Kondo, J Hamabe, K Yamamoto, et al.
American Journal of Medical Genetics|March 1, 1990
Cytogenetic and molecular study of Angelman syndromeK Imaizumi, F Takada, Y Kuroki, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 1, 1979
Hypermotilinemia in chronic renal failureK Shima, A Tanaka, N Sawazaki, et al.
Epilepsia|November 1, 1992
Angelman syndrome in three siblings: characteristic epileptic seizures and EEG abnormalitiesT Sugimoto, A Yasuhara, T Ohta, et al.
American Journal of Medical Genetics|October 1, 1991
DNA deletion and its parental origin in Angelman syndrome patientsJ Hamabe, Y Kuroki, K Imaizumi, et al.
American Journal of Medical Genetics|October 1, 1991
Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patientsJ Hamabe, Y Fukushima, N Harada, et al.
Pageof 1

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

Sort By:
Pageof 1
Nucleic Acids Research|September 25, 1990
StyI polymorphism at the D15S11 locusJ Hamabe, N Niikawa
Nucleic Acids Research|August 25, 1991
A DraI RFLP detected for probe pIR4-3R [D15S11] on chromosome 15qJ Hamabe, N Niikawa
Nucleic Acids Research|September 11, 1991
A BsaBI RFLP detected for probe pML34 [D15S9] on chromosome 15qJ Hamabe, S Saitoh, N Niikawa
Nucleic Acids Research|August 25, 1991
An ApaI RFLP for the human porphobilinogen deaminase gene (PBGD)J Hamabe, H Irifune, N Niikawa
Clinical Genetics|December 1, 1990
Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locusI Kondo, J Hamabe, K Yamamoto, et al.
American Journal of Medical Genetics|March 1, 1990
Cytogenetic and molecular study of Angelman syndromeK Imaizumi, F Takada, Y Kuroki, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 1, 1979
Hypermotilinemia in chronic renal failureK Shima, A Tanaka, N Sawazaki, et al.
Epilepsia|November 1, 1992
Angelman syndrome in three siblings: characteristic epileptic seizures and EEG abnormalitiesT Sugimoto, A Yasuhara, T Ohta, et al.
American Journal of Medical Genetics|October 1, 1991
DNA deletion and its parental origin in Angelman syndrome patientsJ Hamabe, Y Kuroki, K Imaizumi, et al.
American Journal of Medical Genetics|October 1, 1991
Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patientsJ Hamabe, Y Fukushima, N Harada, et al.
Pageof 1