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The Journal of the American Osteopathic Association
|
March 19, 2010
Direct writing electrocardiography
A L PETTIGREW
American Journal of Medical Genetics
|
February 1, 1991
New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease, and seizures
A L Pettigrew, L G Jackson, D H Ledbetter
Human Genetics
|
August 1, 1991
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13
A L Pettigrew, F Greenberg, C T Caskey, et al.
Human Genetics
|
August 1, 1991
Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation center
A L Pettigrew, E R McCabe, F F Elder, et al.
American Journal of Medical Genetics
|
December 1, 1987
Duplication of proximal 15q as a cause of Prader-Willi syndrome
A L Pettigrew, S M Gollin, F Greenberg, et al.
American Journal of Human Genetics
|
December 1, 1991
Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26)
T H Huang, J F Hejtmancik, A Edwards, et al.
Nature
|
January 3, 1991
Localization of the X inactivation centre on the human X chromosome in Xq13
C J Brown, R G Lafreniere, V E Powers, et al.
Leukemia
|
October 6, 2000
The interleukin-3 receptor alpha chain is a unique marker for human acute myelogenous leukemia stem cells
C T Jordan, D Upchurch, S J Szilvassy, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
The Journal of the American Osteopathic Association
|
March 19, 2010
Direct writing electrocardiography
A L PETTIGREW
American Journal of Medical Genetics
|
February 1, 1991
New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease, and seizures
A L Pettigrew, L G Jackson, D H Ledbetter
Human Genetics
|
August 1, 1991
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13
A L Pettigrew, F Greenberg, C T Caskey, et al.
Human Genetics
|
August 1, 1991
Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation center
A L Pettigrew, E R McCabe, F F Elder, et al.
American Journal of Medical Genetics
|
December 1, 1987
Duplication of proximal 15q as a cause of Prader-Willi syndrome
A L Pettigrew, S M Gollin, F Greenberg, et al.
American Journal of Human Genetics
|
December 1, 1991
Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26)
T H Huang, J F Hejtmancik, A Edwards, et al.
Nature
|
January 3, 1991
Localization of the X inactivation centre on the human X chromosome in Xq13
C J Brown, R G Lafreniere, V E Powers, et al.
Leukemia
|
October 6, 2000
The interleukin-3 receptor alpha chain is a unique marker for human acute myelogenous leukemia stem cells
C T Jordan, D Upchurch, S J Szilvassy, et al.
Page
of 1