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Fikret Erdogan

Showing results (11-20 of 21) with videos related to

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Ophthalmic Genetics|March 26, 2008
Blepharophimosis-ptosis-epicanthus inversus syndrome in a girl with chromosome translocation t(2;3)(q33;q23)Andreas Tzschach, Christina Kelbova, Sabine Weidensee, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangementAndreas Tzschach, Corinna Menzel, Fikret Erdogan, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 6, 2008
Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridizationSarah A Shoichet, Stefan Waibel, Sonja Endruhn, et al.
Human Molecular Genetics|November 9, 2007
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophreniaGeorge Kirov, Dilihan Gumus, Wei Chen, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11Andreas Tzschach, Anne-Marie Bisgaard, Maria Kirchhoff, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Chromosome deletions in 13q33-34: report of four patients and review of the literatureJoanna Walczak-Sztulpa, Marzena Wisniewska, Anna Latos-Bielenska, et al.
Human Genetics|January 11, 2007
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardationVera M Kalscheuer, David FitzPatrick, Niels Tommerup, et al.
BMC Cancer|March 24, 2011
Correlation of SHOX2 gene amplification and DNA methylation in lung cancer tumorsKatja U Schneider, Dimo Dietrich, Michael Fleischhacker, et al.
Human Genetics|November 29, 2005
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephalyMasoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, et al.
Genome Research|March 11, 2008
Mapping translocation breakpoints by next-generation sequencingWei Chen, Vera Kalscheuer, Andreas Tzschach, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Ophthalmic Genetics|March 26, 2008
Blepharophimosis-ptosis-epicanthus inversus syndrome in a girl with chromosome translocation t(2;3)(q33;q23)Andreas Tzschach, Christina Kelbova, Sabine Weidensee, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangementAndreas Tzschach, Corinna Menzel, Fikret Erdogan, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 6, 2008
Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridizationSarah A Shoichet, Stefan Waibel, Sonja Endruhn, et al.
Human Molecular Genetics|November 9, 2007
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophreniaGeorge Kirov, Dilihan Gumus, Wei Chen, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11Andreas Tzschach, Anne-Marie Bisgaard, Maria Kirchhoff, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Chromosome deletions in 13q33-34: report of four patients and review of the literatureJoanna Walczak-Sztulpa, Marzena Wisniewska, Anna Latos-Bielenska, et al.
Human Genetics|January 11, 2007
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardationVera M Kalscheuer, David FitzPatrick, Niels Tommerup, et al.
BMC Cancer|March 24, 2011
Correlation of SHOX2 gene amplification and DNA methylation in lung cancer tumorsKatja U Schneider, Dimo Dietrich, Michael Fleischhacker, et al.
Human Genetics|November 29, 2005
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephalyMasoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, et al.
Genome Research|March 11, 2008
Mapping translocation breakpoints by next-generation sequencingWei Chen, Vera Kalscheuer, Andreas Tzschach, et al.
Pageof 3