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O Riess

Showing results (81-90 of 144) with videos related to

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European Journal of Human Genetics : EJHG|April 21, 2001
Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxiaC Zühlke, Y Hellenbroich, A Dalski, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
Characterization of a cosmid library from flow-sorted chromosomes 11B H Weber, H Stöhr, I Siedlaczck, et al.
Prenatal Diagnosis|November 1, 1986
Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysisA Speer, R Bollman, A Michel, et al.
Brain : a Journal of Neurology|April 19, 2002
The aetiology of sporadic adult-onset ataxiaM Abele, K Bürk, L Schöls, et al.
Clinical Genetics|August 29, 2013
PIK3R1 mutations in SHORT syndromeC Schroeder, A Riess, M Bonin, et al.
Brain Research Bulletin|March 28, 2006
Normal sensitivity to excitotoxicity in a transgenic Huntington's disease ratC Winkler, J M A C Gil, I M Araújo, et al.
Epilepsia|July 22, 1998
Replication analysis of a putative susceptibility locus (EGI) for idiopathic generalized epilepsy on chromosome 8q24T Sander, R Kretz, H Schulz, et al.
Neurobiology of Disease|February 10, 2019
Olfactory bulb atrophy and caspase activation observed in the BACHD rat models of Huntington diseaseM Lessard-Beaudoin, L Yu-Taeger, M Laroche, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1995
Machado-Joseph disease mutations as the genetic basis of most spinocerebellar ataxias in GermanyL Schöls, G Amoiridis, M Langkafel, et al.
Epilepsy Research|February 26, 1998
The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsyT Sander, C Peters, D Janz, et al.
Pageof 15

Showing results (81-90 of 144) with videos related to

Sort By:
Pageof 15
European Journal of Human Genetics : EJHG|April 21, 2001
Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxiaC Zühlke, Y Hellenbroich, A Dalski, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
Characterization of a cosmid library from flow-sorted chromosomes 11B H Weber, H Stöhr, I Siedlaczck, et al.
Prenatal Diagnosis|November 1, 1986
Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysisA Speer, R Bollman, A Michel, et al.
Brain : a Journal of Neurology|April 19, 2002
The aetiology of sporadic adult-onset ataxiaM Abele, K Bürk, L Schöls, et al.
Clinical Genetics|August 29, 2013
PIK3R1 mutations in SHORT syndromeC Schroeder, A Riess, M Bonin, et al.
Brain Research Bulletin|March 28, 2006
Normal sensitivity to excitotoxicity in a transgenic Huntington's disease ratC Winkler, J M A C Gil, I M Araújo, et al.
Epilepsia|July 22, 1998
Replication analysis of a putative susceptibility locus (EGI) for idiopathic generalized epilepsy on chromosome 8q24T Sander, R Kretz, H Schulz, et al.
Neurobiology of Disease|February 10, 2019
Olfactory bulb atrophy and caspase activation observed in the BACHD rat models of Huntington diseaseM Lessard-Beaudoin, L Yu-Taeger, M Laroche, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1995
Machado-Joseph disease mutations as the genetic basis of most spinocerebellar ataxias in GermanyL Schöls, G Amoiridis, M Langkafel, et al.
Epilepsy Research|February 26, 1998
The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsyT Sander, C Peters, D Janz, et al.
Pageof 15