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T Darras

Showing results (81-90 of 303) with videos related to

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American Journal of Medical Genetics|June 28, 2001
Exclusion of growth factor gene mutations as a common cause of Sotos syndromeA E Lin, Q Liu, G B Mannheim, et al.
American Journal of Human Genetics|August 1, 1989
Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13U Francke, B T Darras, N F Zander, et al.
Journal of Neuro-Oncology|January 1, 1993
Aggressive oligodendroglioma predicted by chromosome 10 restriction fragment length polymorphism analysis. Case studyJ K Wu, R D Folkerth, Z Ye, et al.
Brain & Development|July 1, 1992
A search for X-chromosome uniparental disomy and DNA rearrangements in the Rett syndromeM J Rivkin, Z Ye, G B Mannheim, et al.
Pediatric Neurology|July 9, 2010
Electrophysiologic evidence for anterior horn cell disease in amyoplasiaJohn N Gaitanis, Hugh J McMillan, Allan Wu, et al.
Neurology|July 13, 2012
Machine learning algorithms to classify spinal muscular atrophy subtypesTuhin Srivastava, Basil T Darras, Jim S Wu, et al.
Genomics|May 1, 1991
Structure of the human cytochrome c oxidase subunit Vb gene and chromosomal mapping of the coding gene and of seven pseudogenesM I Lomax, C L Hsieh, B T Darras, et al.
Journal Belge De Radiologie|January 1, 1977
Endoscopic retrograde pancreatography in the diagnosis of pancreatico-pleural fistulaT Darras, A Gulbis, E Khazzaka, et al.
Chest|June 1, 1972
Intermittent therapy with rifampin once a week in advanced pulmonary tuberculosisL Verbist, S Mbete, H Van Landuyt, et al.
The New England Journal of Medicine|July 2, 2025
Further Comments on Risdiplam for Prenatal Therapy of Spinal Muscular AtrophyCrystal J J Yeo, Darryl C De Vivo, Basil T Darras
Pageof 31

Showing results (81-90 of 303) with videos related to

Sort By:
Pageof 31
American Journal of Medical Genetics|June 28, 2001
Exclusion of growth factor gene mutations as a common cause of Sotos syndromeA E Lin, Q Liu, G B Mannheim, et al.
American Journal of Human Genetics|August 1, 1989
Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13U Francke, B T Darras, N F Zander, et al.
Journal of Neuro-Oncology|January 1, 1993
Aggressive oligodendroglioma predicted by chromosome 10 restriction fragment length polymorphism analysis. Case studyJ K Wu, R D Folkerth, Z Ye, et al.
Brain & Development|July 1, 1992
A search for X-chromosome uniparental disomy and DNA rearrangements in the Rett syndromeM J Rivkin, Z Ye, G B Mannheim, et al.
Pediatric Neurology|July 9, 2010
Electrophysiologic evidence for anterior horn cell disease in amyoplasiaJohn N Gaitanis, Hugh J McMillan, Allan Wu, et al.
Neurology|July 13, 2012
Machine learning algorithms to classify spinal muscular atrophy subtypesTuhin Srivastava, Basil T Darras, Jim S Wu, et al.
Genomics|May 1, 1991
Structure of the human cytochrome c oxidase subunit Vb gene and chromosomal mapping of the coding gene and of seven pseudogenesM I Lomax, C L Hsieh, B T Darras, et al.
Journal Belge De Radiologie|January 1, 1977
Endoscopic retrograde pancreatography in the diagnosis of pancreatico-pleural fistulaT Darras, A Gulbis, E Khazzaka, et al.
Chest|June 1, 1972
Intermittent therapy with rifampin once a week in advanced pulmonary tuberculosisL Verbist, S Mbete, H Van Landuyt, et al.
The New England Journal of Medicine|July 2, 2025
Further Comments on Risdiplam for Prenatal Therapy of Spinal Muscular AtrophyCrystal J J Yeo, Darryl C De Vivo, Basil T Darras
Pageof 31