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

B A Allitto

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Nucleic Acids Research|October 24, 1986
A family of DNA sequences is reproducibly rearranged in the somatic nucleus of TetrahymenaB A Allitto, K M Karrer
Journal of the American Medical Women'S Association (1972)|January 1, 1997
Clinical molecular genetic testingL M Brzustowicz, B A Allitto
Developmental Biology|September 1, 1984
Micronucleus-specific DNA sequences in an amicronucleate mutant of TetrahymenaK Karrer, S Stein-Gavens, B A Allitto
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
Improved detection of cystic fibrosis mutations in the heterogeneous U.S. population using an expanded, pan-ethnic mutation panelR A Heim, E A Sugarman, B A Allitto
Prenatal Diagnosis|July 17, 1998
Fetal echogenic bowel and a dilated loop of bowel associated with cystic fibrosis (CF) mutations delta F508 and 2183AA-->GP W Rush, S Vats, B A Allitto, et al.
American Journal of Obstetrics and Gynecology|September 1, 1984
Quantitation of immunoglobulins in the effusions of human ovarian epithelial neoplasmsW H Kutteh, S A Gall, G J Doellgast, et al.
Obstetrics and Gynecology|July 2, 1999
Cystic fibrosis and chromosome abnormalities associated with echogenic fetal bowelB M Berlin, M E Norton, E A Sugarman, et al.
Nucleic Acids Research|July 25, 1991
Detection by PCR of the VNTR polymorphism at D4S95B A Allitto, G T Horn, M R Altherr, et al.
Molecular and Cellular Probes|December 1, 1992
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4B A Allitto, A I McClatchey, G Barnes, et al.
Genomics|January 1, 1990
Physical maps of 4p16.3, the area expected to contain the Huntington disease mutationM Bućan, M Zimmer, W L Whaley, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|October 24, 1986
A family of DNA sequences is reproducibly rearranged in the somatic nucleus of TetrahymenaB A Allitto, K M Karrer
Journal of the American Medical Women'S Association (1972)|January 1, 1997
Clinical molecular genetic testingL M Brzustowicz, B A Allitto
Developmental Biology|September 1, 1984
Micronucleus-specific DNA sequences in an amicronucleate mutant of TetrahymenaK Karrer, S Stein-Gavens, B A Allitto
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2001
Improved detection of cystic fibrosis mutations in the heterogeneous U.S. population using an expanded, pan-ethnic mutation panelR A Heim, E A Sugarman, B A Allitto
Prenatal Diagnosis|July 17, 1998
Fetal echogenic bowel and a dilated loop of bowel associated with cystic fibrosis (CF) mutations delta F508 and 2183AA-->GP W Rush, S Vats, B A Allitto, et al.
American Journal of Obstetrics and Gynecology|September 1, 1984
Quantitation of immunoglobulins in the effusions of human ovarian epithelial neoplasmsW H Kutteh, S A Gall, G J Doellgast, et al.
Obstetrics and Gynecology|July 2, 1999
Cystic fibrosis and chromosome abnormalities associated with echogenic fetal bowelB M Berlin, M E Norton, E A Sugarman, et al.
Nucleic Acids Research|July 25, 1991
Detection by PCR of the VNTR polymorphism at D4S95B A Allitto, G T Horn, M R Altherr, et al.
Molecular and Cellular Probes|December 1, 1992
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4B A Allitto, A I McClatchey, G Barnes, et al.
Genomics|January 1, 1990
Physical maps of 4p16.3, the area expected to contain the Huntington disease mutationM Bućan, M Zimmer, W L Whaley, et al.
Pageof 2