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T Liehr

Showing results (171-180 of 192) with videos related to

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Cytogenetic and Genome Research|September 29, 2007
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literatureT Liehr, G E Utine, U Trautmann, et al.
Cytogenetic and Genome Research|July 3, 2013
A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossificationR S Guilherme, M C S P Cernach, T E Sfakianakis, et al.
International Journal of Andrology|November 29, 2007
Hypergonadotropic hypogonadism in a patient with inv ins (2;4)A Tzschach, C Ramel, A Kron, et al.
Cytogenetic and Genome Research|September 7, 2006
Multicolor fluorescence in situ hybridization (FISH) applied to FISH-bandingT Liehr, H Starke, A Heller, et al.
Cytogenetic and Genome Research|April 4, 2013
First report of a small supernumerary der(8;14) marker chromosomeR S Guilherme, A R N Dutra, A B A Perez, et al.
Cytogenetic and Genome Research|March 2, 2012
Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown originE Klein, M Rocchi, A Ovens-Raeder, et al.
Human Genetics|March 7, 1998
Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3-q25.2 and mutation analysisK G Michels-Rautenstrauss, C Y Mardin, W M Budde, et al.
Balkan Journal of Medical Genetics : BJMG|November 23, 2013
Human Ring Chromosomes - New Insights for their Clinical SignificanceRs Guilherme, E Klein, Ab Hamid, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literatureT Liehr, K Mrasek, S Hinreiner, et al.
International Journal of Hematology|January 5, 2012
Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11D R Ney-Garcia, T Liehr, S Bhatt, et al.
Pageof 20

Showing results (171-180 of 192) with videos related to

Sort By:
Pageof 20
Cytogenetic and Genome Research|September 29, 2007
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literatureT Liehr, G E Utine, U Trautmann, et al.
Cytogenetic and Genome Research|July 3, 2013
A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossificationR S Guilherme, M C S P Cernach, T E Sfakianakis, et al.
International Journal of Andrology|November 29, 2007
Hypergonadotropic hypogonadism in a patient with inv ins (2;4)A Tzschach, C Ramel, A Kron, et al.
Cytogenetic and Genome Research|September 7, 2006
Multicolor fluorescence in situ hybridization (FISH) applied to FISH-bandingT Liehr, H Starke, A Heller, et al.
Cytogenetic and Genome Research|April 4, 2013
First report of a small supernumerary der(8;14) marker chromosomeR S Guilherme, A R N Dutra, A B A Perez, et al.
Cytogenetic and Genome Research|March 2, 2012
Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown originE Klein, M Rocchi, A Ovens-Raeder, et al.
Human Genetics|March 7, 1998
Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3-q25.2 and mutation analysisK G Michels-Rautenstrauss, C Y Mardin, W M Budde, et al.
Balkan Journal of Medical Genetics : BJMG|November 23, 2013
Human Ring Chromosomes - New Insights for their Clinical SignificanceRs Guilherme, E Klein, Ab Hamid, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literatureT Liehr, K Mrasek, S Hinreiner, et al.
International Journal of Hematology|January 5, 2012
Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11D R Ney-Garcia, T Liehr, S Bhatt, et al.
Pageof 20