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

F Hecht

Showing results (11-20 of 350) with videos related to

Pageof 35
Sort By:
The Journal of Pediatrics|November 1, 1975
Letter: Partial trisomy 15 (dup15q) syndrome and the need for precision in clinical cytogeneticsF Hecht
Cancer Genetics and Cytogenetics|August 1, 1986
The mystery of the stable chromosome with two centromeresF Hecht
Cancer Genetics and Cytogenetics|July 15, 1990
Mapping the gene for X-linked lymphoproliferative diseaseF Hecht
Science (New York, N.Y.)|September 27, 1991
Fragile X geneF Hecht
Cytogenetic and Genome Research|November 15, 2007
Familial cancer syndromes: catalog with commentsF Hecht
Human Genetics|October 1, 1986
Rare, polymorphic, and common fragile sites: a classificationF Hecht
Neurofibromatosis|January 1, 1989
Recognition of neurofibromatosis before von RecklinghausenF Hecht
American Journal of Diseases of Children (1960)|December 1, 1985
Updating a diagnosis. The EEC/EECUT syndromeF Hecht
Clinical Genetics|February 1, 1986
Names in genetics: ban on partial trisomy, tetrasomy and monosomyF Hecht
Cancer Genetics and Cytogenetics|August 1, 1988
Sewall Wright, 98, top geneticistF Hecht
Pageof 35

Showing results (11-20 of 350) with videos related to

Sort By:
Pageof 35
The Journal of Pediatrics|November 1, 1975
Letter: Partial trisomy 15 (dup15q) syndrome and the need for precision in clinical cytogeneticsF Hecht
Cancer Genetics and Cytogenetics|August 1, 1986
The mystery of the stable chromosome with two centromeresF Hecht
Cancer Genetics and Cytogenetics|July 15, 1990
Mapping the gene for X-linked lymphoproliferative diseaseF Hecht
Science (New York, N.Y.)|September 27, 1991
Fragile X geneF Hecht
Cytogenetic and Genome Research|November 15, 2007
Familial cancer syndromes: catalog with commentsF Hecht
Human Genetics|October 1, 1986
Rare, polymorphic, and common fragile sites: a classificationF Hecht
Neurofibromatosis|January 1, 1989
Recognition of neurofibromatosis before von RecklinghausenF Hecht
American Journal of Diseases of Children (1960)|December 1, 1985
Updating a diagnosis. The EEC/EECUT syndromeF Hecht
Clinical Genetics|February 1, 1986
Names in genetics: ban on partial trisomy, tetrasomy and monosomyF Hecht
Cancer Genetics and Cytogenetics|August 1, 1988
Sewall Wright, 98, top geneticistF Hecht
Pageof 35