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 K Bofinger

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
The Journal of Reproductive Medicine|August 12, 1999
45,X/46,X,r(Y) karyotype transmitted by father to son after intracytoplasmic sperm injection for oligospermia. A case reportM K Bofinger, D F Needham, L R Saldana, et al.
Pediatric Research|September 1, 1982
Reduction of cerebrospinal fluid phenylalanine after oral administration of valine, isoleucine, and leucineH K Berry, M K Bofinger, M M Hunt, et al.
Clinical Genetics|June 1, 1983
Comparative diagnostic value of phenylalanine challenge and phenylalanine hydroxylase activity in phenylketonuriaM C Hsieh, H K Berry, M K Bofinger, et al.
American Journal of Medical Genetics|January 1, 1991
A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six casesM K Bofinger, J M Opitz, S W Soukup, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
The Journal of Reproductive Medicine|August 12, 1999
45,X/46,X,r(Y) karyotype transmitted by father to son after intracytoplasmic sperm injection for oligospermia. A case reportM K Bofinger, D F Needham, L R Saldana, et al.
Pediatric Research|September 1, 1982
Reduction of cerebrospinal fluid phenylalanine after oral administration of valine, isoleucine, and leucineH K Berry, M K Bofinger, M M Hunt, et al.
Clinical Genetics|June 1, 1983
Comparative diagnostic value of phenylalanine challenge and phenylalanine hydroxylase activity in phenylketonuriaM C Hsieh, H K Berry, M K Bofinger, et al.
American Journal of Medical Genetics|January 1, 1991
A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six casesM K Bofinger, J M Opitz, S W Soukup, et al.
Pageof 2