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

P N Howard-Peebles

Showing results (41-50 of 91) with videos related to

Pageof 10
Sort By:
American Journal of Human Genetics|March 1, 1979
Familial X-linked mental retardation, verbal disability, and marker X chromosomesP N Howard-Peebles, G R Stoddard, M G Mims
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1982
Hemifacial microsomia in cri du chat (5p-) syndromeK W Neu, J M Friedman, P N Howard-Peebles
American Journal of Medical Genetics|September 1, 1992
Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segmentJ M Friedman, M J Harrod, P N Howard-Peebles
American Journal of Medical Genetics|June 1, 1985
Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocationK Bauer, P N Howard-Peebles, D Keele, et al.
Lancet (London, England)|March 20, 1993
Population screening for fragile-X syndromeP N Howard-Peebles, A Maddalena, S H Black, et al.
Molecular and Cellular Biology|December 1, 1990
Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangementR Wevrick, W C Earnshaw, P N Howard-Peebles, et al.
American Journal of Medical Genetics|August 9, 1996
A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in bloodA Maddalena, K N Yadvish, W C Spence, et al.
The Journal of Heredity|May 1, 1980
Analysis of a marine fish cell line from a male sheepsheadP E Gregory, P N Howard-Peebles, R D Ellender, et al.
Clinical Genetics|January 1, 1977
Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12)P N Howard-Peebles, K M Yarbrough, G R Stoddard, et al.
American Journal of Medical Genetics|August 1, 1986
del(20p) with manifestations of arteriohepatic dysplasiaJ L Byrne, M J Harrod, J M Friedman, et al.
Pageof 10

Showing results (41-50 of 91) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|March 1, 1979
Familial X-linked mental retardation, verbal disability, and marker X chromosomesP N Howard-Peebles, G R Stoddard, M G Mims
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1982
Hemifacial microsomia in cri du chat (5p-) syndromeK W Neu, J M Friedman, P N Howard-Peebles
American Journal of Medical Genetics|September 1, 1992
Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segmentJ M Friedman, M J Harrod, P N Howard-Peebles
American Journal of Medical Genetics|June 1, 1985
Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocationK Bauer, P N Howard-Peebles, D Keele, et al.
Lancet (London, England)|March 20, 1993
Population screening for fragile-X syndromeP N Howard-Peebles, A Maddalena, S H Black, et al.
Molecular and Cellular Biology|December 1, 1990
Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangementR Wevrick, W C Earnshaw, P N Howard-Peebles, et al.
American Journal of Medical Genetics|August 9, 1996
A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in bloodA Maddalena, K N Yadvish, W C Spence, et al.
The Journal of Heredity|May 1, 1980
Analysis of a marine fish cell line from a male sheepsheadP E Gregory, P N Howard-Peebles, R D Ellender, et al.
Clinical Genetics|January 1, 1977
Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12)P N Howard-Peebles, K M Yarbrough, G R Stoddard, et al.
American Journal of Medical Genetics|August 1, 1986
del(20p) with manifestations of arteriohepatic dysplasiaJ L Byrne, M J Harrod, J M Friedman, et al.
Pageof 10