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S J Kirkpatrick

Showing results (11-20 of 21) with videos related to

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American Journal of Medical Genetics|April 1, 1994
Wisconsin Stillbirth Service Program: I. Establishment and assessment of a community-based program for etiologic investigation of intrauterine deathsR M Pauli, C A Reiser, R M Lebovitz, et al.
Journal of Biomedical Materials Research|November 6, 2002
Mechanical properties of coagulated albumin and failure mechanisms of liver repaired with the use of an argon-beam coagulator with albuminT P Moffitt, D A Baker, S J Kirkpatrick, et al.
Applied Optics|October 12, 2010
Transform method of processing for speckle strain-rate measurementsD D Duncan, S J Kirkpatrick, F F Mark, et al.
Teratology|April 1, 1992
Further evidence that arthrogryposis multiplex congenita in the human sometimes is caused by an intrauterine vascular accidentW L Robertson, L P Glinski, S J Kirkpatrick, et al.
The Biochemical Journal|November 1, 1971
Effect of chemical modification of tyrosine residues on bone morphogenesisB S Strates, S J Kirkpatrick, J E Heffner, et al.
Photochemistry and Photobiology|July 1, 1995
The development of personal dosimeters for use in the visible and ultraviolet wavelengths regions. The Salisbury Eye Evaluation TeamD D Duncan, W Schneider, K J West, et al.
Clinical Genetics|December 1, 1982
Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocationR M Pauli, S J Kirkpatrick, L F Meisner, et al.
Genomics|September 1, 1991
Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this regionE W Jabs, C A Coss, S J Hayflick, et al.
Human Mutation|October 26, 1999
Homonucleotide expansion and contraction mutations of PAX2 and inclusion of Chiari 1 malformation as part of renal-coloboma syndromeL A Schimmenti, H H Shim, J D Wirtschafter, et al.
American Journal of Human Genetics|January 1, 1997
Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23B E Baysal, J E Farr, W S Rubinstein, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|April 1, 1994
Wisconsin Stillbirth Service Program: I. Establishment and assessment of a community-based program for etiologic investigation of intrauterine deathsR M Pauli, C A Reiser, R M Lebovitz, et al.
Journal of Biomedical Materials Research|November 6, 2002
Mechanical properties of coagulated albumin and failure mechanisms of liver repaired with the use of an argon-beam coagulator with albuminT P Moffitt, D A Baker, S J Kirkpatrick, et al.
Applied Optics|October 12, 2010
Transform method of processing for speckle strain-rate measurementsD D Duncan, S J Kirkpatrick, F F Mark, et al.
Teratology|April 1, 1992
Further evidence that arthrogryposis multiplex congenita in the human sometimes is caused by an intrauterine vascular accidentW L Robertson, L P Glinski, S J Kirkpatrick, et al.
The Biochemical Journal|November 1, 1971
Effect of chemical modification of tyrosine residues on bone morphogenesisB S Strates, S J Kirkpatrick, J E Heffner, et al.
Photochemistry and Photobiology|July 1, 1995
The development of personal dosimeters for use in the visible and ultraviolet wavelengths regions. The Salisbury Eye Evaluation TeamD D Duncan, W Schneider, K J West, et al.
Clinical Genetics|December 1, 1982
Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocationR M Pauli, S J Kirkpatrick, L F Meisner, et al.
Genomics|September 1, 1991
Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this regionE W Jabs, C A Coss, S J Hayflick, et al.
Human Mutation|October 26, 1999
Homonucleotide expansion and contraction mutations of PAX2 and inclusion of Chiari 1 malformation as part of renal-coloboma syndromeL A Schimmenti, H H Shim, J D Wirtschafter, et al.
American Journal of Human Genetics|January 1, 1997
Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23B E Baysal, J E Farr, W S Rubinstein, et al.
Pageof 3