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A Baumer

Showing results (11-20 of 63) with videos related to

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Prenatal Diagnosis|December 11, 1999
Severe intra-uterine growth retardation in a patient with maternal uniparental disomy 22 and a 22-trisomic placentaD Balmer, A Baumer, B Röthlisberger, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Parental origin and mechanisms of formation of triploidy: a study of 25 casesA Baumer, D Balmer, F Binkert, et al.
Biological Psychiatry|April 15, 1997
Apolipoprotein E-epsilon 4 allele frequency in late-onset depressionA Heidrich, J Thome, M Rösler, et al.
Human Mutation|April 24, 2001
A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicismsA Baumer, U Wiedemann, M Hergersberg, et al.
Mutation Research|September 1, 1992
Mitochondrial DNA mutation and the ageing process: bioenergy and pharmacological interventionA W Linnane, C Zhang, A Baumer, et al.
American Journal of Human Genetics|April 1, 1994
Age-related human mtDNA deletions: a heterogeneous set of deletions arising at a single pair of directly repeated sequencesA Baumer, C Zhang, A W Linnane, et al.
European Journal of Human Genetics : EJHG|July 6, 2000
An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian familyA Baumer, S Belli, R M Trüeb, et al.
Human Genetics|August 1, 1996
New mutations in the ataxia telangiectasia geneA Baumer, U Bernthaler, W Wolz, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Isochromosomes 12p and 9p: parental origin and possible mechanisms of formationF Dutly, D Balmer, A Baumer, et al.
Journal of Neural Transmission. Parkinson'S Disease and Dementia Section|January 1, 1995
Alpha-1-antichymotrypsin bi-allele polymorphism, apolipoprotein-E tri-allele polymorphism and genetic risk of Alzheimer's syndromeJ Thome, A Baumer, J Kornhuber, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|December 11, 1999
Severe intra-uterine growth retardation in a patient with maternal uniparental disomy 22 and a 22-trisomic placentaD Balmer, A Baumer, B Röthlisberger, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Parental origin and mechanisms of formation of triploidy: a study of 25 casesA Baumer, D Balmer, F Binkert, et al.
Biological Psychiatry|April 15, 1997
Apolipoprotein E-epsilon 4 allele frequency in late-onset depressionA Heidrich, J Thome, M Rösler, et al.
Human Mutation|April 24, 2001
A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicismsA Baumer, U Wiedemann, M Hergersberg, et al.
Mutation Research|September 1, 1992
Mitochondrial DNA mutation and the ageing process: bioenergy and pharmacological interventionA W Linnane, C Zhang, A Baumer, et al.
American Journal of Human Genetics|April 1, 1994
Age-related human mtDNA deletions: a heterogeneous set of deletions arising at a single pair of directly repeated sequencesA Baumer, C Zhang, A W Linnane, et al.
European Journal of Human Genetics : EJHG|July 6, 2000
An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian familyA Baumer, S Belli, R M Trüeb, et al.
Human Genetics|August 1, 1996
New mutations in the ataxia telangiectasia geneA Baumer, U Bernthaler, W Wolz, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Isochromosomes 12p and 9p: parental origin and possible mechanisms of formationF Dutly, D Balmer, A Baumer, et al.
Journal of Neural Transmission. Parkinson'S Disease and Dementia Section|January 1, 1995
Alpha-1-antichymotrypsin bi-allele polymorphism, apolipoprotein-E tri-allele polymorphism and genetic risk of Alzheimer's syndromeJ Thome, A Baumer, J Kornhuber, et al.
Pageof 7