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M P Short

Showing results (51-60 of 64) with videos related to

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American Journal of Medical Genetics|March 1, 1987
Cholesteryl ester storage disease: pathologic changes in an affected fetusP K Desai, K H Astrin, S N Thung, et al.
Birth Defects Original Article Series|January 1, 1986
Bone marrow transplantation in Maroteaux-Lamy syndrome (MPS type 6): status 40 months after BMTM M McGovern, M D Ludman, M P Short, et al.
The Review of Scientific Instruments|February 11, 2025
Accelerating plasma and radiation surface science using transient grating spectroscopyA P C Wylie, K B Woller, M Rae, et al.
Brain Research. Molecular Brain Research|June 1, 1989
Grafting genetically modified cells into the rat brain: characteristics of E. coli beta-galactosidase as a reporter geneS Shimohama, M B Rosenberg, A M Fagan, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Clinical findings and linkage studies in familial tuberous sclerosisM P Short, J Haines, A Jewell, et al.
The New England Journal of Medicine|October 3, 1996
Clinical and biochemical manifestations of hyaluronidase deficiencyM R Natowicz, M P Short, Y Wang, et al.
American Journal of Human Genetics|August 1, 1996
Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesionsE P Henske, B W Scheithauer, M P Short, et al.
American Journal of Human Genetics|October 1, 1991
Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneityJ L Haines, M P Short, D J Kwiatkowski, et al.
Nature Genetics|September 1, 1992
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney diseaseR S Kandt, J L Haines, M Smith, et al.
American Journal of Human Genetics|August 1, 1994
Mutational analysis of patients with neurofibromatosis 2M MacCollin, V Ramesh, L B Jacoby, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|March 1, 1987
Cholesteryl ester storage disease: pathologic changes in an affected fetusP K Desai, K H Astrin, S N Thung, et al.
Birth Defects Original Article Series|January 1, 1986
Bone marrow transplantation in Maroteaux-Lamy syndrome (MPS type 6): status 40 months after BMTM M McGovern, M D Ludman, M P Short, et al.
The Review of Scientific Instruments|February 11, 2025
Accelerating plasma and radiation surface science using transient grating spectroscopyA P C Wylie, K B Woller, M Rae, et al.
Brain Research. Molecular Brain Research|June 1, 1989
Grafting genetically modified cells into the rat brain: characteristics of E. coli beta-galactosidase as a reporter geneS Shimohama, M B Rosenberg, A M Fagan, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Clinical findings and linkage studies in familial tuberous sclerosisM P Short, J Haines, A Jewell, et al.
The New England Journal of Medicine|October 3, 1996
Clinical and biochemical manifestations of hyaluronidase deficiencyM R Natowicz, M P Short, Y Wang, et al.
American Journal of Human Genetics|August 1, 1996
Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesionsE P Henske, B W Scheithauer, M P Short, et al.
American Journal of Human Genetics|October 1, 1991
Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneityJ L Haines, M P Short, D J Kwiatkowski, et al.
Nature Genetics|September 1, 1992
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney diseaseR S Kandt, J L Haines, M Smith, et al.
American Journal of Human Genetics|August 1, 1994
Mutational analysis of patients with neurofibromatosis 2M MacCollin, V Ramesh, L B Jacoby, et al.
Pageof 7