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

R L Neu

Showing results (41-50 of 58) with videos related to

Pageof 6
Sort By:
British Medical Journal|March 31, 1979
Minor hazard of amniocentesisR L Neu, J T Lanman, M Wingate, et al.
Journal of Medical Genetics|March 1, 1970
48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosomeG J Bargman, R L Neu, H O Powers, et al.
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|March 1, 1972
Giemsa staining of heterochromatic areas of human chromosomes for identificationJ P Frey, R L Neu, H O Powers, et al.
Journal of Medical Genetics|August 1, 1976
46,XY/46,XY,21q- mosaicism in an infant with neutropenia and properdin deficiencyR L Neu, J A Stockman, R E Spitzer, et al.
Annales De Genetique|January 1, 1979
An infant with trisomy 9pter yields 9q22 resulting from 3:1 segregation in a 46,XX t(1;9) (p36;q22) motherR L Neu, N R Dennis, J T Lanman, et al.
Journal of Medical Genetics|March 1, 1970
A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-)G J Bargman, R L Neu, H O Powers, et al.
Journal of Medical Genetics|March 1, 1973
Three generations and six family members with a t(13q15q) chromosomeR L Neu, L I Gardner, M L Williams, et al.
Clinical Genetics|September 1, 1992
Cleft palate and complex chromosome rearrangementsB G Kousseff, P Papenhausen, R L Neu, et al.
Annales De Genetique|January 1, 1981
An infant with trisomy 6q21 leads to 6qterR L Neu, J U Gallien, N Steinberg-Warren, et al.
American Journal of Medical Genetics|January 1, 1981
Brief clinical report: an infant with duplication of 17q21 lead to 17qterJ U Gallien, R L Neu, R J Wynn, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
British Medical Journal|March 31, 1979
Minor hazard of amniocentesisR L Neu, J T Lanman, M Wingate, et al.
Journal of Medical Genetics|March 1, 1970
48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosomeG J Bargman, R L Neu, H O Powers, et al.
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|March 1, 1972
Giemsa staining of heterochromatic areas of human chromosomes for identificationJ P Frey, R L Neu, H O Powers, et al.
Journal of Medical Genetics|August 1, 1976
46,XY/46,XY,21q- mosaicism in an infant with neutropenia and properdin deficiencyR L Neu, J A Stockman, R E Spitzer, et al.
Annales De Genetique|January 1, 1979
An infant with trisomy 9pter yields 9q22 resulting from 3:1 segregation in a 46,XX t(1;9) (p36;q22) motherR L Neu, N R Dennis, J T Lanman, et al.
Journal of Medical Genetics|March 1, 1970
A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-)G J Bargman, R L Neu, H O Powers, et al.
Journal of Medical Genetics|March 1, 1973
Three generations and six family members with a t(13q15q) chromosomeR L Neu, L I Gardner, M L Williams, et al.
Clinical Genetics|September 1, 1992
Cleft palate and complex chromosome rearrangementsB G Kousseff, P Papenhausen, R L Neu, et al.
Annales De Genetique|January 1, 1981
An infant with trisomy 6q21 leads to 6qterR L Neu, J U Gallien, N Steinberg-Warren, et al.
American Journal of Medical Genetics|January 1, 1981
Brief clinical report: an infant with duplication of 17q21 lead to 17qterJ U Gallien, R L Neu, R J Wynn, et al.
Pageof 6