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H Leonard

Showing results (211-220 of 236) with videos related to

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Physics in Medicine and Biology|October 10, 2012
Comparison of breast tissue measurements using magnetic resonance imaging, digital mammography and a mathematical algorithmLee-Jane W Lu, Thomas K Nishino, Raleigh F Johnson, et al.
Neurology|March 12, 2008
Investigating genotype-phenotype relationships in Rett syndrome using an international data setA Bebbington, A Anderson, D Ravine, et al.
Journal of Medical Genetics|November 17, 2009
Updating the profile of C-terminal MECP2 deletions in Rett syndromeA Bebbington, A Percy, J Christodoulou, et al.
Journal of Autism and Developmental Disorders|December 21, 2006
Development of a video-based evaluation tool in Rett syndromeS Fyfe, J Downs, O McIlroy, et al.
Annals of the New York Academy of Sciences|July 10, 2003
Genetic association and cellular function of MC1R variant alleles in human pigmentationR A Sturm, D L Duffy, N F Box, et al.
Clinical Genetics|December 21, 2011
What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?J Zhang, X Bao, G Cao, et al.
Oncogene|March 2, 2011
Inverse expression states of the BRN2 and MITF transcription factors in melanoma spheres and tumour xenografts regulate the NOTCH pathwayA E Thurber, G Douglas, E C Sturm, et al.
American Journal of Hospital Pharmacy|October 1, 1990
Multi-institutional drug-use evaluation of intraocular irrigating solutionsR G Closson, C A Biggio, L Childress, et al.
Journal of Pediatric Surgery|May 4, 2005
Survival of severe congenital diaphragmatic hernia has morbid consequencesRaul A Cortes, Roberta L Keller, Tiffany Townsend, et al.
Journal of Medical Genetics|May 15, 2003
Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?H Leonard, L Colvin, J Christodoulou, et al.
Pageof 24

Showing results (211-220 of 236) with videos related to

Sort By:
Pageof 24
Physics in Medicine and Biology|October 10, 2012
Comparison of breast tissue measurements using magnetic resonance imaging, digital mammography and a mathematical algorithmLee-Jane W Lu, Thomas K Nishino, Raleigh F Johnson, et al.
Neurology|March 12, 2008
Investigating genotype-phenotype relationships in Rett syndrome using an international data setA Bebbington, A Anderson, D Ravine, et al.
Journal of Medical Genetics|November 17, 2009
Updating the profile of C-terminal MECP2 deletions in Rett syndromeA Bebbington, A Percy, J Christodoulou, et al.
Journal of Autism and Developmental Disorders|December 21, 2006
Development of a video-based evaluation tool in Rett syndromeS Fyfe, J Downs, O McIlroy, et al.
Annals of the New York Academy of Sciences|July 10, 2003
Genetic association and cellular function of MC1R variant alleles in human pigmentationR A Sturm, D L Duffy, N F Box, et al.
Clinical Genetics|December 21, 2011
What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?J Zhang, X Bao, G Cao, et al.
Oncogene|March 2, 2011
Inverse expression states of the BRN2 and MITF transcription factors in melanoma spheres and tumour xenografts regulate the NOTCH pathwayA E Thurber, G Douglas, E C Sturm, et al.
American Journal of Hospital Pharmacy|October 1, 1990
Multi-institutional drug-use evaluation of intraocular irrigating solutionsR G Closson, C A Biggio, L Childress, et al.
Journal of Pediatric Surgery|May 4, 2005
Survival of severe congenital diaphragmatic hernia has morbid consequencesRaul A Cortes, Roberta L Keller, Tiffany Townsend, et al.
Journal of Medical Genetics|May 15, 2003
Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?H Leonard, L Colvin, J Christodoulou, et al.
Pageof 24