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K Eggermann

Showing results (21-30 of 33) with videos related to

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European Journal of Medical Genetics|August 15, 2006
Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISHA Roos, S Rudnik-Schöneborn, K Eggermann, et al.
Journal of Medical Genetics|February 7, 2001
Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patientsT Eggermann, S Mergenthaler, K Eggermann, et al.
Journal of Medical Genetics|October 21, 2005
Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domainT Eggermann, N Schönherr, E Meyer, et al.
Annales De Genetique|May 20, 2000
Formation of uniparental disomy 7 delineated from new cases and a UPD7 case after trisomy 7 rescue. Presentation of own results and review of the literatureS Mergenthaler, H A Wollmann, B Burger, et al.
Clinical Genetics|April 7, 2005
Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qterT Eggermann, D Meschede, H Schüler, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|November 1, 1996
Efficacy and side-effects of clozapine: testing for association with allelic variation in the dopamine D4 receptor geneM Rietschel, D Naber, H Oberländer, et al.
American Journal of Human Genetics|October 1, 1995
Association analysis of the monoamine oxidase A gene in bipolar affective disorder by using family-based internal controlsM M Nöthen, K Eggermann, M Albus, et al.
Journal of Medical Genetics|July 30, 2008
Congenital heart disease is a feature of severe infantile spinal muscular atrophyS Rudnik-Schöneborn, R Heller, C Berg, et al.
Clinical Genetics|September 29, 2009
Genotype-phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counsellingS Rudnik-Schöneborn, C Berg, K Zerres, et al.
Clinical Nephrology|May 31, 2002
Analysis of the genes SLC7A9 and SLC3A1 in unclassified cystinurics: mutation detection rates and association between variants in SLC7A9 and the diseaseC Schmidt, A Albers, J Tomiuk, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
European Journal of Medical Genetics|August 15, 2006
Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISHA Roos, S Rudnik-Schöneborn, K Eggermann, et al.
Journal of Medical Genetics|February 7, 2001
Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patientsT Eggermann, S Mergenthaler, K Eggermann, et al.
Journal of Medical Genetics|October 21, 2005
Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domainT Eggermann, N Schönherr, E Meyer, et al.
Annales De Genetique|May 20, 2000
Formation of uniparental disomy 7 delineated from new cases and a UPD7 case after trisomy 7 rescue. Presentation of own results and review of the literatureS Mergenthaler, H A Wollmann, B Burger, et al.
Clinical Genetics|April 7, 2005
Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qterT Eggermann, D Meschede, H Schüler, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|November 1, 1996
Efficacy and side-effects of clozapine: testing for association with allelic variation in the dopamine D4 receptor geneM Rietschel, D Naber, H Oberländer, et al.
American Journal of Human Genetics|October 1, 1995
Association analysis of the monoamine oxidase A gene in bipolar affective disorder by using family-based internal controlsM M Nöthen, K Eggermann, M Albus, et al.
Journal of Medical Genetics|July 30, 2008
Congenital heart disease is a feature of severe infantile spinal muscular atrophyS Rudnik-Schöneborn, R Heller, C Berg, et al.
Clinical Genetics|September 29, 2009
Genotype-phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counsellingS Rudnik-Schöneborn, C Berg, K Zerres, et al.
Clinical Nephrology|May 31, 2002
Analysis of the genes SLC7A9 and SLC3A1 in unclassified cystinurics: mutation detection rates and association between variants in SLC7A9 and the diseaseC Schmidt, A Albers, J Tomiuk, et al.
Pageof 4