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N J Mendelsohn

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American Journal of Medical Genetics|May 9, 2001
Unique case of trisomy 2p24.3-pter with no associated monosomyJ A Roggenbuck, J M Fink, N J Mendelsohn
The American Journal of Cardiology|March 15, 1993
Detection and assessment by positron emission tomography of a genetically determined defect in myocardial fatty acid utilization (long-chain acyl-CoA dehydrogenase deficiency)D P Kelly, N J Mendelsohn, B E Sobel, et al.
Pediatric Radiology|January 1, 1991
Microcephalic osteodysplastic primordial dwarfism, type II. Report of a case with characteristic skeletal featuresT E Herman, N J Mendelsohn, S B Dowton, et al.
Biochimica Et Biophysica Acta|January 3, 1997
Regulation of the human long chain acyl-CoA dehydrogenase gene by nuclear hormone receptor transcription factorsZ Zhang, Y Zhou, N J Mendelsohn, et al.
Pediatric Research|November 1, 1993
Expression and characterization of human mutant (glutamic acid304) medium-chain acyl-coenzyme A dehydrogenase in mammalian cellsA J Whelan, A W Strauss, D E Hale, et al.
Journal of Genetic Counseling|November 5, 2015
Erratum to: The Long and Short of Genetic Counseling Letters: A Case-control StudyJ Roggenbuck, R Temme, D Pond, et al.
Journal of Genetic Counseling|December 16, 2014
The Long and Short of Genetic Counseling Summary Letters: A Case-control StudyJ Roggenbuck, R Temme, D Pond, et al.
Genes, Brain, and Behavior|December 17, 2008
Genotype differences in cognitive functioning in Noonan syndromeE I Pierpont, M E Pierpont, N J Mendelsohn, et al.
American Journal of Medical Genetics. Part A|July 3, 2009
A synonymous mutation in TCOF1 causes Treacher Collins syndrome due to mis-splicing of a constitutive exonD Macaya, S H Katsanis, T W Hefferon, et al.
American Journal of Medical Genetics|May 22, 1995
Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two casesL A Schimmenti, R R Higgins, N J Mendelsohn, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|May 9, 2001
Unique case of trisomy 2p24.3-pter with no associated monosomyJ A Roggenbuck, J M Fink, N J Mendelsohn
The American Journal of Cardiology|March 15, 1993
Detection and assessment by positron emission tomography of a genetically determined defect in myocardial fatty acid utilization (long-chain acyl-CoA dehydrogenase deficiency)D P Kelly, N J Mendelsohn, B E Sobel, et al.
Pediatric Radiology|January 1, 1991
Microcephalic osteodysplastic primordial dwarfism, type II. Report of a case with characteristic skeletal featuresT E Herman, N J Mendelsohn, S B Dowton, et al.
Biochimica Et Biophysica Acta|January 3, 1997
Regulation of the human long chain acyl-CoA dehydrogenase gene by nuclear hormone receptor transcription factorsZ Zhang, Y Zhou, N J Mendelsohn, et al.
Pediatric Research|November 1, 1993
Expression and characterization of human mutant (glutamic acid304) medium-chain acyl-coenzyme A dehydrogenase in mammalian cellsA J Whelan, A W Strauss, D E Hale, et al.
Journal of Genetic Counseling|November 5, 2015
Erratum to: The Long and Short of Genetic Counseling Letters: A Case-control StudyJ Roggenbuck, R Temme, D Pond, et al.
Journal of Genetic Counseling|December 16, 2014
The Long and Short of Genetic Counseling Summary Letters: A Case-control StudyJ Roggenbuck, R Temme, D Pond, et al.
Genes, Brain, and Behavior|December 17, 2008
Genotype differences in cognitive functioning in Noonan syndromeE I Pierpont, M E Pierpont, N J Mendelsohn, et al.
American Journal of Medical Genetics. Part A|July 3, 2009
A synonymous mutation in TCOF1 causes Treacher Collins syndrome due to mis-splicing of a constitutive exonD Macaya, S H Katsanis, T W Hefferon, et al.
American Journal of Medical Genetics|May 22, 1995
Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two casesL A Schimmenti, R R Higgins, N J Mendelsohn, et al.
Pageof 2