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Neuropsychologia
|
February 26, 2000
Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment
D V Bishop, E Canning, K Elgar, et al.
Human Molecular Genetics
|
March 1, 1996
Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome
E E Eichler, J N Macpherson, A Murray, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1994
A systematic search for uniparental disomy in carriers of chromosome translocations
R S James, I K Temple, C Patch, et al.
Journal of Medical Genetics
|
June 1, 1993
Population studies of the fragile X: a molecular approach
P A Jacobs, H Bullman, J Macpherson, et al.
Annals of Human Genetics
|
May 1, 1988
Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes
P A Jacobs, T J Hassold, E Whittington, et al.
Annals of Human Genetics
|
January 1, 1990
A centromere map of the X chromosome from trisomies of maternal origin
N E Morton, B J Keats, P A Jacobs, et al.
American Journal of Human Genetics
|
July 1, 1982
Expression of the marker (X) (q28) in lymphoblastoid cell lines
P A Jacobs, P A Hunt, M Mayer, et al.
Cytogenetics and Cell Genetics
|
January 1, 1986
Cytogenetic analysis of lymphoblastoid cell lines
M A Abruzzo, P A Hunt, M Mayer, et al.
American Journal of Human Genetics
|
April 1, 1986
A comparison of fragile X expression in lymphocyte and lymphoblastoid cultures
M A Abruzzo, P A Hunt, M Mayer, et al.
American Journal of Human Genetics
|
April 1, 1990
The parental origin of the extra X chromosome in 47,XXX females
K M May, P A Jacobs, M Lee, et al.
Page
of 14
Search research articles
Search
Showing results (91-100 of 136) with videos related to
Sort By:
Page
of 14
Neuropsychologia
|
February 26, 2000
Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment
D V Bishop, E Canning, K Elgar, et al.
Human Molecular Genetics
|
March 1, 1996
Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome
E E Eichler, J N Macpherson, A Murray, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1994
A systematic search for uniparental disomy in carriers of chromosome translocations
R S James, I K Temple, C Patch, et al.
Journal of Medical Genetics
|
June 1, 1993
Population studies of the fragile X: a molecular approach
P A Jacobs, H Bullman, J Macpherson, et al.
Annals of Human Genetics
|
May 1, 1988
Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes
P A Jacobs, T J Hassold, E Whittington, et al.
Annals of Human Genetics
|
January 1, 1990
A centromere map of the X chromosome from trisomies of maternal origin
N E Morton, B J Keats, P A Jacobs, et al.
American Journal of Human Genetics
|
July 1, 1982
Expression of the marker (X) (q28) in lymphoblastoid cell lines
P A Jacobs, P A Hunt, M Mayer, et al.
Cytogenetics and Cell Genetics
|
January 1, 1986
Cytogenetic analysis of lymphoblastoid cell lines
M A Abruzzo, P A Hunt, M Mayer, et al.
American Journal of Human Genetics
|
April 1, 1986
A comparison of fragile X expression in lymphocyte and lymphoblastoid cultures
M A Abruzzo, P A Hunt, M Mayer, et al.
American Journal of Human Genetics
|
April 1, 1990
The parental origin of the extra X chromosome in 47,XXX females
K M May, P A Jacobs, M Lee, et al.
Page
of 14