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 E Ferguson

Showing results (11-20 of 24) with videos related to

Pageof 3
Sort By:
Prenatal Diagnosis|October 1, 1990
Prenatal diagnosis of a double bisatellited marker with an unusual copy number ratioJ J Waters, M E Ferguson-Smith, N Carter, et al.
Prenatal Diagnosis|November 1, 1994
Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective studyD H Spathas, A Divane, G M Maniatis, et al.
Cytometry|January 1, 1990
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blotsN P Carter, M E Ferguson-Smith, N A Affara, et al.
Human Genetics|October 1, 1988
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?J L Tolmie, E Boyd, P Batstone, et al.
Scientific Reports|August 31, 2017
A time series transcriptome analysis of cassava (Manihot esculenta Crantz) varieties challenged with Ugandan cassava brown streak virusT Amuge, D K Berger, M S Katari, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|April 7, 2004
Microsatellite identification and characterization in peanut ( A. hypogaea L.)M E Ferguson, M D Burow, S R Schulze, et al.
Journal of Medical Genetics|February 1, 1986
Early prenatal investigation of a pregnancy at risk of adenosine deaminase deficiency using chorionic villiD A Aitken, D H Gilmore, C A Frew, et al.
Prenatal Diagnosis|November 1, 1992
Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contigY L Zheng, M A Ferguson-Smith, J P Warner, et al.
Journal of Medical Genetics|October 1, 1992
A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell lineL R Willatt, B C Davison, D Goudie, et al.
Prenatal Diagnosis|May 1, 1994
Second-trimester maternal serum screening using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: experience of a regional programmeS F Goodburn, J R Yates, P R Raggatt, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|October 1, 1990
Prenatal diagnosis of a double bisatellited marker with an unusual copy number ratioJ J Waters, M E Ferguson-Smith, N Carter, et al.
Prenatal Diagnosis|November 1, 1994
Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective studyD H Spathas, A Divane, G M Maniatis, et al.
Cytometry|January 1, 1990
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blotsN P Carter, M E Ferguson-Smith, N A Affara, et al.
Human Genetics|October 1, 1988
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?J L Tolmie, E Boyd, P Batstone, et al.
Scientific Reports|August 31, 2017
A time series transcriptome analysis of cassava (Manihot esculenta Crantz) varieties challenged with Ugandan cassava brown streak virusT Amuge, D K Berger, M S Katari, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|April 7, 2004
Microsatellite identification and characterization in peanut ( A. hypogaea L.)M E Ferguson, M D Burow, S R Schulze, et al.
Journal of Medical Genetics|February 1, 1986
Early prenatal investigation of a pregnancy at risk of adenosine deaminase deficiency using chorionic villiD A Aitken, D H Gilmore, C A Frew, et al.
Prenatal Diagnosis|November 1, 1992
Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contigY L Zheng, M A Ferguson-Smith, J P Warner, et al.
Journal of Medical Genetics|October 1, 1992
A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell lineL R Willatt, B C Davison, D Goudie, et al.
Prenatal Diagnosis|May 1, 1994
Second-trimester maternal serum screening using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: experience of a regional programmeS F Goodburn, J R Yates, P R Raggatt, et al.
Pageof 3