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A Stephan

Showing results (171-180 of 223) with videos related to

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European Journal of Human Genetics : EJHG|June 15, 2006
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairmentNanna D Rendtorff, Mei Zhu, Toril Fagerheim, et al.
Human Molecular Genetics|February 13, 2001
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)N Tiso, D A Stephan, A Nava, et al.
Molecular Psychiatry|December 21, 2006
Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14D Q Ma, M L Cuccaro, J M Jaworski, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 26, 2006
High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35Demetra S Stamm, Evadnie Rampersaud, Susan H Slifer, et al.
Mitochondrion|August 22, 2006
Quantitation of heteroplasmy of mtDNA sequence variants identified in a population of AD patients and controls by array-based resequencingKeith D Coon, Jon Valla, Szabolics Szelinger, et al.
The American Journal of Drug and Alcohol Abuse|October 8, 2016
Meta-analyses of clinical neuropsychological tests of executive dysfunction and impulsivity in alcohol use disorderRick A Stephan, Omar M Alhassoon, Kenneth E Allen, et al.
Journal of Alzheimer'S Disease : JAD|August 18, 2006
Preliminary demonstration of an allelic association of the IREB2 gene with Alzheimer's diseaseKeith D Coon, Andrew M Siegel, Stephanie J Yee, et al.
The International Journal of Neuropsychopharmacology|August 16, 2005
Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorderJobst Meyer, Kirsten Johannssen, Christine M Freitag, et al.
Transplantation Proceedings|March 12, 2004
The pharmacokinetics of equoral versus neoral in stable renal transplant patients: a multinational multicenter studyM A Masri, M Haberal, A Rizvi, et al.
Molecular Genetics and Metabolism|June 2, 2000
Positional cloning utilizing genomic DNA microarrays: the Niemann-Pick type C gene as a model systemD A Stephan, Y Chen, Y Jiang, et al.
Pageof 23

Showing results (171-180 of 223) with videos related to

Sort By:
Pageof 23
European Journal of Human Genetics : EJHG|June 15, 2006
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairmentNanna D Rendtorff, Mei Zhu, Toril Fagerheim, et al.
Human Molecular Genetics|February 13, 2001
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)N Tiso, D A Stephan, A Nava, et al.
Molecular Psychiatry|December 21, 2006
Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14D Q Ma, M L Cuccaro, J M Jaworski, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 26, 2006
High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35Demetra S Stamm, Evadnie Rampersaud, Susan H Slifer, et al.
Mitochondrion|August 22, 2006
Quantitation of heteroplasmy of mtDNA sequence variants identified in a population of AD patients and controls by array-based resequencingKeith D Coon, Jon Valla, Szabolics Szelinger, et al.
The American Journal of Drug and Alcohol Abuse|October 8, 2016
Meta-analyses of clinical neuropsychological tests of executive dysfunction and impulsivity in alcohol use disorderRick A Stephan, Omar M Alhassoon, Kenneth E Allen, et al.
Journal of Alzheimer'S Disease : JAD|August 18, 2006
Preliminary demonstration of an allelic association of the IREB2 gene with Alzheimer's diseaseKeith D Coon, Andrew M Siegel, Stephanie J Yee, et al.
The International Journal of Neuropsychopharmacology|August 16, 2005
Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorderJobst Meyer, Kirsten Johannssen, Christine M Freitag, et al.
Transplantation Proceedings|March 12, 2004
The pharmacokinetics of equoral versus neoral in stable renal transplant patients: a multinational multicenter studyM A Masri, M Haberal, A Rizvi, et al.
Molecular Genetics and Metabolism|June 2, 2000
Positional cloning utilizing genomic DNA microarrays: the Niemann-Pick type C gene as a model systemD A Stephan, Y Chen, Y Jiang, et al.
Pageof 23