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

W Wertelecki

Showing results (61-70 of 85) with videos related to

Pageof 9
Sort By:
Mutation Research|July 1, 1995
Repair of mitochondrial DNA damage induced by bleomycin in human cellsC C Shen, W Wertelecki, W J Driggers, et al.
American Journal of Medical Genetics|May 17, 1996
A complex five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspringC M Tuck-Muller, M Varela, S Li, et al.
American Journal of Medical Genetics|June 5, 1995
Translocation 10;18 in a patient with juvenile neuronal ceroid-lipofuscinosis (Batten disease)C M Tuck-Muller, P R Dyken, S Li, et al.
Human Genetics|May 1, 1993
Duplication of the short arm of the X chromosome in mother and daughterC M Tuck-Muller, J E Martinez, D A Batista, et al.
American Journal of Medical Genetics|March 1, 1986
Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmataW Wertelecki, W R Breg, J M Graham, et al.
Birth Defects Original Article Series|January 1, 1982
Comparative studies of infants with mosaic and complete triploidy: an analysis of 55 casesW R Blackburn, W P Miller, D W Superneau, et al.
American Journal of Medical Genetics|January 8, 1999
Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH)S Li, C M Tuck-Muller, J E Martínez, et al.
American Journal of Medical Genetics|March 1, 1994
Confirmation of proximal 1q duplication using fluorescence in situ hybridizationH Chen, C J Kusyk, C M Tuck-Muller, et al.
Social Science & Medicine (1982)|January 1, 1985
Maternal sociomedical characteristics and birth weights of firstbornsC Hoff, W Wertelecki, E Reyes, et al.
Southern Medical Journal|July 6, 2000
FGFR3 gene mutation (Gly380Arg) with achondroplasia and i(21q) Down syndrome: phenotype-genotype correlationH Chen, X Mu, T Sonoda, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Mutation Research|July 1, 1995
Repair of mitochondrial DNA damage induced by bleomycin in human cellsC C Shen, W Wertelecki, W J Driggers, et al.
American Journal of Medical Genetics|May 17, 1996
A complex five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspringC M Tuck-Muller, M Varela, S Li, et al.
American Journal of Medical Genetics|June 5, 1995
Translocation 10;18 in a patient with juvenile neuronal ceroid-lipofuscinosis (Batten disease)C M Tuck-Muller, P R Dyken, S Li, et al.
Human Genetics|May 1, 1993
Duplication of the short arm of the X chromosome in mother and daughterC M Tuck-Muller, J E Martinez, D A Batista, et al.
American Journal of Medical Genetics|March 1, 1986
Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmataW Wertelecki, W R Breg, J M Graham, et al.
Birth Defects Original Article Series|January 1, 1982
Comparative studies of infants with mosaic and complete triploidy: an analysis of 55 casesW R Blackburn, W P Miller, D W Superneau, et al.
American Journal of Medical Genetics|January 8, 1999
Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH)S Li, C M Tuck-Muller, J E Martínez, et al.
American Journal of Medical Genetics|March 1, 1994
Confirmation of proximal 1q duplication using fluorescence in situ hybridizationH Chen, C J Kusyk, C M Tuck-Muller, et al.
Social Science & Medicine (1982)|January 1, 1985
Maternal sociomedical characteristics and birth weights of firstbornsC Hoff, W Wertelecki, E Reyes, et al.
Southern Medical Journal|July 6, 2000
FGFR3 gene mutation (Gly380Arg) with achondroplasia and i(21q) Down syndrome: phenotype-genotype correlationH Chen, X Mu, T Sonoda, et al.
Pageof 9