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Genomics
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January 25, 2000
Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig
L O Maddox, M M Menold, M P Bass, et al.
Journal of Medical Genetics
|
October 1, 1995
Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B
J R Gilbert, M C Speer, J Stajich, et al.
Genomics
|
August 1, 1992
Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis
F Samson, P J de Jong, B J Trask, et al.
Neurogenetics
|
March 25, 2000
Further exclusion of FSHD1B from the telomeric region of 10q
M C Speer, M A Pericak-Vance, J M Stajich, et al.
Journal of Natural Products
|
June 28, 2000
Ribofuranosyl triazolone: a natural product herbicide with activity on adenylosuccinate synthetase following phosphorylation
P R Schmitzer, P R Graupner, E L Chapin, et al.
Human Heredity
|
February 25, 2000
Physical and cDNA mapping in the DBH region of human chromosome 9q34
J R Gilbert, A Kumar, S Newey, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
April 1, 1998
Bioavailability and pharmacokinetics of microencapsulated 1,3-dichloropropene in rats
W T Stott, J R Gilbert, R J McGuirk, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 11, 2009
Inhibition of thromboxane A2-induced arrhythmias and intracellular calcium changes in cardiac myocytes by blockade of the inositol trisphosphate pathway
M J Wacker, L M Kosloski, W J R Gilbert, et al.
JAMA
|
January 24, 1986
Does a mailed continuing education program improve physician performance? Results of a randomized trial in antihypertensive care
C E Evans, R B Haynes, N J Birkett, et al.
American Journal of Medical Genetics
|
July 18, 2000
Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome
S L Donnelly, C M Wolpert, M M Menold, et al.
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of 12
Search research articles
Search
Showing results (61-70 of 120) with videos related to
Sort By:
Page
of 12
Genomics
|
January 25, 2000
Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig
L O Maddox, M M Menold, M P Bass, et al.
Journal of Medical Genetics
|
October 1, 1995
Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B
J R Gilbert, M C Speer, J Stajich, et al.
Genomics
|
August 1, 1992
Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis
F Samson, P J de Jong, B J Trask, et al.
Neurogenetics
|
March 25, 2000
Further exclusion of FSHD1B from the telomeric region of 10q
M C Speer, M A Pericak-Vance, J M Stajich, et al.
Journal of Natural Products
|
June 28, 2000
Ribofuranosyl triazolone: a natural product herbicide with activity on adenylosuccinate synthetase following phosphorylation
P R Schmitzer, P R Graupner, E L Chapin, et al.
Human Heredity
|
February 25, 2000
Physical and cDNA mapping in the DBH region of human chromosome 9q34
J R Gilbert, A Kumar, S Newey, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
April 1, 1998
Bioavailability and pharmacokinetics of microencapsulated 1,3-dichloropropene in rats
W T Stott, J R Gilbert, R J McGuirk, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
September 11, 2009
Inhibition of thromboxane A2-induced arrhythmias and intracellular calcium changes in cardiac myocytes by blockade of the inositol trisphosphate pathway
M J Wacker, L M Kosloski, W J R Gilbert, et al.
JAMA
|
January 24, 1986
Does a mailed continuing education program improve physician performance? Results of a randomized trial in antihypertensive care
C E Evans, R B Haynes, N J Birkett, et al.
American Journal of Medical Genetics
|
July 18, 2000
Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome
S L Donnelly, C M Wolpert, M M Menold, et al.
Page
of 12