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TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 5, 2013

Construction and characterisation of a yeast artificial chromosome library containing five haploid sugarbeet (Beta vulgaris L.) genome equivalentsJ Del-Favero, M Vauterin, G Weyens, et al.

TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 12, 2013

Highly asymmetric intergeneric nuclear hybrids between Nicotiana and Petunia: evidence for recombinogenic and translocation events in somatic hybrid plants after "gamma"-fusionS Hinnisdaels, L Bariller, A Mouras, et al.

Brain Research Bulletin|November 24, 2001

Trinucleotide repeat expansions: do they contribute to bipolar disorder?D Goossens, J Del-Favero, C Van Broeckhoven

Human Genetics|December 22, 1999

Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degenerationA Michalík, J Del-Favero, C Mauger, et al.

Gene|March 30, 1999

YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14J Del-Favero, D Goossens, D Van den Bossche, et al.

Journal of the Neurological Sciences|September 29, 1999

Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian familyJ Martin, N Van Regemorter, J Del-Favero, et al.

Psychopharmacology|February 8, 2016

Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in DrosophilaL Herteleer, L Zwarts, K Hens, et al.

Brain Research. Molecular Brain Research|January 21, 2000

Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibodyC Mauger, J Del-Favero, C Ceuterick, et al.

American Journal of Human Genetics|May 19, 2001

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancyL Claes, J Del-Favero, B Ceulemans, et al.

Journal of Biochemical and Molecular Toxicology|October 4, 2007

Gene expression analysis of estrogenic compounds in the liver of common carp (Cyprinus carpio) using a custom cDNA microarrayLotte N Moens, K van der Ven, P Van Remortel, et al.

Pageof 250

Showing results (1-10 of 2,498) with videos related to

Sort By:

Pageof 250

TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 5, 2013

Construction and characterisation of a yeast artificial chromosome library containing five haploid sugarbeet (Beta vulgaris L.) genome equivalentsJ Del-Favero, M Vauterin, G Weyens, et al.

TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 12, 2013

Highly asymmetric intergeneric nuclear hybrids between Nicotiana and Petunia: evidence for recombinogenic and translocation events in somatic hybrid plants after "gamma"-fusionS Hinnisdaels, L Bariller, A Mouras, et al.

Brain Research Bulletin|November 24, 2001

Trinucleotide repeat expansions: do they contribute to bipolar disorder?D Goossens, J Del-Favero, C Van Broeckhoven

Human Genetics|December 22, 1999

Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degenerationA Michalík, J Del-Favero, C Mauger, et al.

Gene|March 30, 1999

YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14J Del-Favero, D Goossens, D Van den Bossche, et al.

Journal of the Neurological Sciences|September 29, 1999

Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian familyJ Martin, N Van Regemorter, J Del-Favero, et al.

Psychopharmacology|February 8, 2016

Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in DrosophilaL Herteleer, L Zwarts, K Hens, et al.

Brain Research. Molecular Brain Research|January 21, 2000

Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibodyC Mauger, J Del-Favero, C Ceuterick, et al.

American Journal of Human Genetics|May 19, 2001

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancyL Claes, J Del-Favero, B Ceulemans, et al.

Journal of Biochemical and Molecular Toxicology|October 4, 2007

Gene expression analysis of estrogenic compounds in the liver of common carp (Cyprinus carpio) using a custom cDNA microarrayLotte N Moens, K van der Ven, P Van Remortel, et al.

Pageof 250