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E C Jenkins

Showing results (31-40 of 146) with videos related to

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Clinical Genetics|February 1, 1983
Monosomy 21 syndrome: further delineation including clinical, neuropathological, cytogenetic and biochemical studiesK Wisniewski, M Dambska, E C Jenkins, et al.
American Journal of Medical Genetics|May 1, 1988
In situ nick translation of the fragile X regionS L Nolin, E C Jenkins, W T Brown, et al.
Human Genetics|January 1, 1985
Genetic linkage heterogeneity in the fragile X syndromeW T Brown, A C Gross, C B Chan, et al.
American Journal of Medical Genetics|February 1, 1991
Transformation and establishment of fragile X cell lines from amniocytesL S Jenkins, D C Gruenert, E C Jenkins, et al.
Annales De Genetique|June 1, 1975
De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girlE C Jenkins, F M Curcuru-Giordano, S G Krishna, et al.
American Journal of Medical Genetics|January 1, 1986
Fragile X expression increased by low cell-culture densityM S Krawczun, K P Lele, E C Jenkins, et al.
Cytogenetics and Cell Genetics|January 1, 1976
A child with presumptive monosomy 21 (45,XY,-21) in a family in which some members are Gq-J G Davis, E C Jenkins, H P Klinger, et al.
American Journal of Medical Genetics|May 1, 1988
Screening developmentally disabled male populations for fragile X: the effect of sample sizeG S Fisch, I L Cohen, E C Jenkins, et al.
American Journal of Medical Genetics|January 1, 1986
DNA linkage studies in the fragile X syndrome suggest genetic heterogeneityW T Brown, A C Gross, C B Chan, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X expression in short-term whole blood cultures is affected by cell densityM S Krawczun, E C Jenkins, W T Brown, et al.
Pageof 15

Showing results (31-40 of 146) with videos related to

Sort By:
Pageof 15
Clinical Genetics|February 1, 1983
Monosomy 21 syndrome: further delineation including clinical, neuropathological, cytogenetic and biochemical studiesK Wisniewski, M Dambska, E C Jenkins, et al.
American Journal of Medical Genetics|May 1, 1988
In situ nick translation of the fragile X regionS L Nolin, E C Jenkins, W T Brown, et al.
Human Genetics|January 1, 1985
Genetic linkage heterogeneity in the fragile X syndromeW T Brown, A C Gross, C B Chan, et al.
American Journal of Medical Genetics|February 1, 1991
Transformation and establishment of fragile X cell lines from amniocytesL S Jenkins, D C Gruenert, E C Jenkins, et al.
Annales De Genetique|June 1, 1975
De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girlE C Jenkins, F M Curcuru-Giordano, S G Krishna, et al.
American Journal of Medical Genetics|January 1, 1986
Fragile X expression increased by low cell-culture densityM S Krawczun, K P Lele, E C Jenkins, et al.
Cytogenetics and Cell Genetics|January 1, 1976
A child with presumptive monosomy 21 (45,XY,-21) in a family in which some members are Gq-J G Davis, E C Jenkins, H P Klinger, et al.
American Journal of Medical Genetics|May 1, 1988
Screening developmentally disabled male populations for fragile X: the effect of sample sizeG S Fisch, I L Cohen, E C Jenkins, et al.
American Journal of Medical Genetics|January 1, 1986
DNA linkage studies in the fragile X syndrome suggest genetic heterogeneityW T Brown, A C Gross, C B Chan, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X expression in short-term whole blood cultures is affected by cell densityM S Krawczun, E C Jenkins, W T Brown, et al.
Pageof 15