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M M Cohen

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Genomics|January 1, 1994
Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7pA F Lewanda, M M Cohen, C E Jackson, et al.
American Journal of Medical Genetics|October 1, 1993
Saethre-Chotzen syndrome with familial translocation at chromosome 7p22C S Reid, L E McMorrow, D M McDonald-McGinn, et al.
IEEE Transactions on Medical Imaging|November 10, 2001
Enhancement of contrast echocardiography by image variability analysisB J Fetics, E Y Wong, T Murabayashi, et al.
American Journal of Hematology|April 1, 1985
Increased numbers of marrow basophils may be associated with a t(6;9) in ANLLM G Pearson, J W Vardiman, M M Le Beau, et al.
Medical Care|December 1, 1995
A population-based health information systemN P Roos, C D Black, N Frohlich, et al.
The Journal of Pediatrics|February 1, 1986
Further delineation of Weaver syndromeH H Ardinger, J W Hanson, M J Harrod, et al.
Nature Genetics|August 1, 1996
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndromeK A Przylepa, W Paznekas, M Zhang, et al.
QJM : Monthly Journal of the Association of Physicians|July 19, 2011
Use of variability in national and regional data to estimate the prevalence of lymphangioleiomyomatosisE C Harknett, W Y C Chang, S Byrnes, et al.
Human Molecular Genetics|September 25, 1997
A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22G J Feldman, D E Ward, E Lajeunie-Renier, et al.
American Journal of Human Genetics|March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.
Pageof 45

Showing results (441-450 of 450) with videos related to

Sort By:
Pageof 45
You have reached the last page of results.This site can display upto 450 results.
Genomics|January 1, 1994
Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7pA F Lewanda, M M Cohen, C E Jackson, et al.
American Journal of Medical Genetics|October 1, 1993
Saethre-Chotzen syndrome with familial translocation at chromosome 7p22C S Reid, L E McMorrow, D M McDonald-McGinn, et al.
IEEE Transactions on Medical Imaging|November 10, 2001
Enhancement of contrast echocardiography by image variability analysisB J Fetics, E Y Wong, T Murabayashi, et al.
American Journal of Hematology|April 1, 1985
Increased numbers of marrow basophils may be associated with a t(6;9) in ANLLM G Pearson, J W Vardiman, M M Le Beau, et al.
Medical Care|December 1, 1995
A population-based health information systemN P Roos, C D Black, N Frohlich, et al.
The Journal of Pediatrics|February 1, 1986
Further delineation of Weaver syndromeH H Ardinger, J W Hanson, M J Harrod, et al.
Nature Genetics|August 1, 1996
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndromeK A Przylepa, W Paznekas, M Zhang, et al.
QJM : Monthly Journal of the Association of Physicians|July 19, 2011
Use of variability in national and regional data to estimate the prevalence of lymphangioleiomyomatosisE C Harknett, W Y C Chang, S Byrnes, et al.
Human Molecular Genetics|September 25, 1997
A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22G J Feldman, D E Ward, E Lajeunie-Renier, et al.
American Journal of Human Genetics|March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeM Muenke, K W Gripp, D M McDonald-McGinn, et al.
Pageof 45