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

S C Finley

Showing results (11-20 of 47) with videos related to

Pageof 5
Sort By:
The Alabama Journal of Medical Sciences|October 1, 1984
First trimester prenatal diagnosis of genetic disorders. Will chorionic villi sampling make it a reality?P Cosper, S C Finley, R W Quinlan
Journal of Medical Genetics|September 1, 1971
An extra small metacentric chromosome in association with multiple congenital abnormalitiesW H Finley, S C Finley, D Monsky
Journal of Medical Genetics|April 1, 1986
An additional case of Smith-Lemli-Opitz syndrome in a 46,XY infant with female external genitaliaP R Scarbrough, K Huddleston, S C Finley
Southern Medical Journal|June 1, 1973
Clinical features associated with the chromosomal deletion syndrome manifested by an 18 ring (46,18r)D M Brasfield, S C Finley, W H Finley
Southern Medical Journal|August 1, 1983
Psychiatric disturbances in a 6-year-old boy with Klinefelter's syndromeC E McDanal, S C Finley, W H Finley
Clinical Genetics|November 1, 1975
Fetal loss and familial chromosome 1 translocationsJ H Garrett, S C Finley, W H Finley
The Alabama Journal of Medical Sciences|April 1, 1982
A review of trisomies 21, 18, and 13P R Scarbrough, W H Finley, S C Finley
American Journal of Human Genetics|April 1, 1987
Survey of medical genetics personnelW H Finley, S C Finley, R L Dyer
The Alabama Journal of Medical Sciences|January 1, 1984
Fragile-X syndrome. An overviewP R Scarbrough, P Cosper, S C Finley, et al.
Journal of Medical Genetics|April 1, 1986
Partial trisomy 6p and partial trisomy 22 resulting from 3:1 meiotic disjunction of maternal (6p;22q) translocationP R Scarbrough, A J Carroll, S C Finley, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
The Alabama Journal of Medical Sciences|October 1, 1984
First trimester prenatal diagnosis of genetic disorders. Will chorionic villi sampling make it a reality?P Cosper, S C Finley, R W Quinlan
Journal of Medical Genetics|September 1, 1971
An extra small metacentric chromosome in association with multiple congenital abnormalitiesW H Finley, S C Finley, D Monsky
Journal of Medical Genetics|April 1, 1986
An additional case of Smith-Lemli-Opitz syndrome in a 46,XY infant with female external genitaliaP R Scarbrough, K Huddleston, S C Finley
Southern Medical Journal|June 1, 1973
Clinical features associated with the chromosomal deletion syndrome manifested by an 18 ring (46,18r)D M Brasfield, S C Finley, W H Finley
Southern Medical Journal|August 1, 1983
Psychiatric disturbances in a 6-year-old boy with Klinefelter's syndromeC E McDanal, S C Finley, W H Finley
Clinical Genetics|November 1, 1975
Fetal loss and familial chromosome 1 translocationsJ H Garrett, S C Finley, W H Finley
The Alabama Journal of Medical Sciences|April 1, 1982
A review of trisomies 21, 18, and 13P R Scarbrough, W H Finley, S C Finley
American Journal of Human Genetics|April 1, 1987
Survey of medical genetics personnelW H Finley, S C Finley, R L Dyer
The Alabama Journal of Medical Sciences|January 1, 1984
Fragile-X syndrome. An overviewP R Scarbrough, P Cosper, S C Finley, et al.
Journal of Medical Genetics|April 1, 1986
Partial trisomy 6p and partial trisomy 22 resulting from 3:1 meiotic disjunction of maternal (6p;22q) translocationP R Scarbrough, A J Carroll, S C Finley, et al.
Pageof 5