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B T Darras

Showing results (21-30 of 55) with videos related to

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American Journal of Medical Genetics|March 1, 1988
Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNAB T Darras, M Koenig, L M Kunkel, et al.
Blood|August 1, 1990
Origin of mutations in two families with X-linked chronic granulomatous diseaseU Francke, H D Ochs, B T Darras, et al.
Journal of Neuro-Oncology|January 1, 1994
Clonal analysis of human astrocytomasR P Morse, B T Darras, Z Ye, et al.
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.
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.
Pediatric Neurology|March 1, 1989
Intermittent dystonia in Hartnup diseaseB T Darras, M G Ampola, W H Dietz, et al.
Clinical Genetics|June 7, 2003
XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's diseaseJ M Milunsky, T A Maher, B A Loose, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|March 1, 1988
Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNAB T Darras, M Koenig, L M Kunkel, et al.
Blood|August 1, 1990
Origin of mutations in two families with X-linked chronic granulomatous diseaseU Francke, H D Ochs, B T Darras, et al.
Journal of Neuro-Oncology|January 1, 1994
Clonal analysis of human astrocytomasR P Morse, B T Darras, Z Ye, et al.
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.
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.
Pediatric Neurology|March 1, 1989
Intermittent dystonia in Hartnup diseaseB T Darras, M G Ampola, W H Dietz, et al.
Clinical Genetics|June 7, 2003
XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's diseaseJ M Milunsky, T A Maher, B A Loose, et al.
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