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 G Wilson

Showing results (91-100 of 388) with videos related to

Pageof 39
Sort By:
Human Heredity|January 1, 1994
A rare 6q11+ heteromorphism: cytogenetic analysis and in situ hybridizationM S Lin, A Zhang, A Fujimoto, et al.
American Journal of Medical Genetics|January 1, 1979
Syndromes associated with deletion of the long arm of chromosome 18[del(18q)]M G Wilson, J W Towner, I Forsman, et al.
Nature|June 11, 1971
Identification of an unusual Y chromosome in YY mosaicism by quinacrine fluorescenceM G Wilson, J W Towner, J Lipshin, et al.
Human Genetics|February 16, 1978
A fetus with recombinant of chromosome 8 inherited from her carrier fatherA Fujimoto, J W Towner, S B Turkel, et al.
Journal of Medical Genetics|September 1, 1973
Trisomy 13 in two infants with cyclopsA Fujimoto, A J Ebbin, J W Towner, et al.
Clinical Genetics|January 1, 1990
Lack of specificity of DA/DAPI fluorescenceM S Lin, K H Huynh, A Fujimoto, et al.
Journal of Medical Genetics|December 1, 1971
An inherited 1;G translocationA J Ebbin, M G Wilson, J W Towner, et al.
Lancet (London, England)|June 7, 1975
Letter: 46,XX/47,XYY mosaicism in a true hermaphroditeM Buyse, D Fordney-Settlage, J W Towner, et al.
American Journal of Medical Genetics|March 1, 1983
Nonimmune fetal hydrops and Down syndromeA Fujimoto, D L Broom, N W Shinno, et al.
Lancet (London, England)|September 27, 1975
Letter: Needle puncture of the fetus during amniocentesisD L Broome, B Kellogg, B A Weiss, et al.
Pageof 39

Showing results (91-100 of 388) with videos related to

Sort By:
Pageof 39
Human Heredity|January 1, 1994
A rare 6q11+ heteromorphism: cytogenetic analysis and in situ hybridizationM S Lin, A Zhang, A Fujimoto, et al.
American Journal of Medical Genetics|January 1, 1979
Syndromes associated with deletion of the long arm of chromosome 18[del(18q)]M G Wilson, J W Towner, I Forsman, et al.
Nature|June 11, 1971
Identification of an unusual Y chromosome in YY mosaicism by quinacrine fluorescenceM G Wilson, J W Towner, J Lipshin, et al.
Human Genetics|February 16, 1978
A fetus with recombinant of chromosome 8 inherited from her carrier fatherA Fujimoto, J W Towner, S B Turkel, et al.
Journal of Medical Genetics|September 1, 1973
Trisomy 13 in two infants with cyclopsA Fujimoto, A J Ebbin, J W Towner, et al.
Clinical Genetics|January 1, 1990
Lack of specificity of DA/DAPI fluorescenceM S Lin, K H Huynh, A Fujimoto, et al.
Journal of Medical Genetics|December 1, 1971
An inherited 1;G translocationA J Ebbin, M G Wilson, J W Towner, et al.
Lancet (London, England)|June 7, 1975
Letter: 46,XX/47,XYY mosaicism in a true hermaphroditeM Buyse, D Fordney-Settlage, J W Towner, et al.
American Journal of Medical Genetics|March 1, 1983
Nonimmune fetal hydrops and Down syndromeA Fujimoto, D L Broom, N W Shinno, et al.
Lancet (London, England)|September 27, 1975
Letter: Needle puncture of the fetus during amniocentesisD L Broome, B Kellogg, B A Weiss, et al.
Pageof 39