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H Northrup

Showing results (41-50 of 68) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990
Electrostatic field around cytochrome c: theory and energy transfer experimentS H Northrup, T G Wensel, C F Meares, et al.
Journal of Medical Genetics|January 14, 2000
Mutational analysis of the tuberous sclerosis gene TSC2 in patients with pulmonary lymphangioleiomyomatosisA Astrinidis, L Khare, T Carsillo, et al.
Human Mutation|January 1, 1997
Mutations and polymorphisms in the tuberous sclerosis complex gene on chromosome 16K S Au, J A Rodriguez, E Rodriguez, et al.
American Journal of Human Genetics|March 26, 1999
Germ-line mosaicism in tuberous sclerosis: how common?V M Rose, K S Au, G Pollom, et al.
Genomics|October 1, 1989
Multilocus linkage analysis with the human argininosuccinate synthetase geneH Northrup, M Lathrop, S Y Lu, et al.
Pediatric Neurosurgery|July 9, 1998
On the surgical treatment of refractory epilepsy in tuberous sclerosis complexJ E Baumgartner, J W Wheless, S Kulkarni, et al.
Journal of Medical Genetics|January 15, 2003
Identification of a mutation in the Indian Hedgehog (IHH) gene causing brachydactyly type A1 and evidence for a third locusT J Kirkpatrick, K-S Au, J M Mastrobattista, et al.
Lancet (London, England)|October 3, 1987
Linkage of tuberous sclerosis to ABO blood groupH Northrup, A L Beaudet, W E O'Brien, et al.
Neuropediatrics|April 1, 1996
Cobblestone lissencephaly with normal eyes and muscleW B Dobyns, M A Patton, R F Stratton, et al.
American Journal of Medical Genetics|July 13, 2002
Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defectsK A Volcik, S H Blanton, M C Kruzel, et al.
Pageof 7

Showing results (41-50 of 68) with videos related to

Sort By:
Pageof 7
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990
Electrostatic field around cytochrome c: theory and energy transfer experimentS H Northrup, T G Wensel, C F Meares, et al.
Journal of Medical Genetics|January 14, 2000
Mutational analysis of the tuberous sclerosis gene TSC2 in patients with pulmonary lymphangioleiomyomatosisA Astrinidis, L Khare, T Carsillo, et al.
Human Mutation|January 1, 1997
Mutations and polymorphisms in the tuberous sclerosis complex gene on chromosome 16K S Au, J A Rodriguez, E Rodriguez, et al.
American Journal of Human Genetics|March 26, 1999
Germ-line mosaicism in tuberous sclerosis: how common?V M Rose, K S Au, G Pollom, et al.
Genomics|October 1, 1989
Multilocus linkage analysis with the human argininosuccinate synthetase geneH Northrup, M Lathrop, S Y Lu, et al.
Pediatric Neurosurgery|July 9, 1998
On the surgical treatment of refractory epilepsy in tuberous sclerosis complexJ E Baumgartner, J W Wheless, S Kulkarni, et al.
Journal of Medical Genetics|January 15, 2003
Identification of a mutation in the Indian Hedgehog (IHH) gene causing brachydactyly type A1 and evidence for a third locusT J Kirkpatrick, K-S Au, J M Mastrobattista, et al.
Lancet (London, England)|October 3, 1987
Linkage of tuberous sclerosis to ABO blood groupH Northrup, A L Beaudet, W E O'Brien, et al.
Neuropediatrics|April 1, 1996
Cobblestone lissencephaly with normal eyes and muscleW B Dobyns, M A Patton, R F Stratton, et al.
American Journal of Medical Genetics|July 13, 2002
Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defectsK A Volcik, S H Blanton, M C Kruzel, et al.
Pageof 7