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 J Pettenati

Showing results (1-10 of 87) with videos related to

Pageof 9
Sort By:
Human Genetics|June 1, 1991
Triple trisomy in a 17-week-old fetusM J Pettenati, N Rao
American Journal of Medical Genetics|May 5, 2001
Maternal homozygosity for the common MTHFR mutation as a potential risk factor for offspring with limb defectsV Shashi, A Rickheim, M J Pettenati
American Journal of Medical Genetics|October 1, 1989
Translocation t(5;11)(q13.1;p13) associated with familial isolated aniridiaM J Pettenati, R G Weaver, B K Burton
Obstetrics and Gynecology|January 1, 1990
Risk of fetal chromosomal anomalies in patients with elevated maternal serum alpha-fetoproteinA A Warner, M J Pettenati, B K Burton
American Journal of Medical Genetics|May 1, 1986
Diploid-triploid mosaicism: report of necropsy findingsM J Pettenati, L D Mirkin, D J Goldstein
Cancer Genetics and Cytogenetics|February 1, 1989
Translocation of the MOS gene in a rare t(8;16) associated with acute myeloblastic leukemia and Down syndromeM J Pettenati, J W McNay, A R Chauvenet
Obstetrics and Gynecology|October 1, 1989
False-positive acetylcholinesterase with early amniocentesisB K Burton, L H Nelson, M J Pettenati
Clinical Genetics|January 1, 1994
Prenatal detection of cri du chat syndrome on uncultured amniocytes using fluorescence in situ hybridization (FISH)M J Pettenati, R Hayworth, K Cox, et al.
American Journal of Medical Genetics|August 10, 1999
Partial duplication of 4q12q13 leads to a mild phenotypeV Shashi, M N Berry, C Santos, et al.
Archives of Pathology & Laboratory Medicine|July 11, 2000
Identification of female cells in postcoital penile swabs using fluorescence in situ hybridizationK A Collins, M S Cina, M J Pettenati, et al.
Pageof 9

Showing results (1-10 of 87) with videos related to

Sort By:
Pageof 9
Human Genetics|June 1, 1991
Triple trisomy in a 17-week-old fetusM J Pettenati, N Rao
American Journal of Medical Genetics|May 5, 2001
Maternal homozygosity for the common MTHFR mutation as a potential risk factor for offspring with limb defectsV Shashi, A Rickheim, M J Pettenati
American Journal of Medical Genetics|October 1, 1989
Translocation t(5;11)(q13.1;p13) associated with familial isolated aniridiaM J Pettenati, R G Weaver, B K Burton
Obstetrics and Gynecology|January 1, 1990
Risk of fetal chromosomal anomalies in patients with elevated maternal serum alpha-fetoproteinA A Warner, M J Pettenati, B K Burton
American Journal of Medical Genetics|May 1, 1986
Diploid-triploid mosaicism: report of necropsy findingsM J Pettenati, L D Mirkin, D J Goldstein
Cancer Genetics and Cytogenetics|February 1, 1989
Translocation of the MOS gene in a rare t(8;16) associated with acute myeloblastic leukemia and Down syndromeM J Pettenati, J W McNay, A R Chauvenet
Obstetrics and Gynecology|October 1, 1989
False-positive acetylcholinesterase with early amniocentesisB K Burton, L H Nelson, M J Pettenati
Clinical Genetics|January 1, 1994
Prenatal detection of cri du chat syndrome on uncultured amniocytes using fluorescence in situ hybridization (FISH)M J Pettenati, R Hayworth, K Cox, et al.
American Journal of Medical Genetics|August 10, 1999
Partial duplication of 4q12q13 leads to a mild phenotypeV Shashi, M N Berry, C Santos, et al.
Archives of Pathology & Laboratory Medicine|July 11, 2000
Identification of female cells in postcoital penile swabs using fluorescence in situ hybridizationK A Collins, M S Cina, M J Pettenati, et al.
Pageof 9