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Heike Starke

Showing results (31-40 of 39) with videos related to

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International Journal of Oncology|June 7, 2003
Highly complex karyotypic changes in acute myelogenous leukemia: a case reportAnita Heller, Nikolai Rubtsov, Soili Kytölä, et al.
Molecular Cytogenetics|June 2, 2009
Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cellsJörn Erlecke, Isabell Hartmann, Martin Hoffmann, et al.
European Journal of Pediatrics|June 24, 2003
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literatureJörg Seidel, Anita Heller, Gabriele Senger, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
Karyotyping of human synaptonemal complexes by cenM-FISHMaria Oliver-Bonet, Thomas Liehr, Angela Nietzel, et al.
European Journal of Medical Genetics|September 24, 2005
Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotypeJoris Robert Vermeesch, Cindy Melotte, Ivo Salden, et al.
Journal of the Association of Genetic Technologists|June 24, 2004
Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic ApproachesThomas Liehr, Angela Nietzel, Heike Starke, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangementsHeike Starke, Jörg Seidel, Wolfram Henn, et al.
Clinical Dysmorphology|September 13, 2005
Three new cases with a supernumerary ring chromosome 1Laura Rodríguez, Heike Starke, Nieves Martínez Guardia, et al.
Human Genetics|September 19, 2003
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classificationHeike Starke, Angela Nietzel, Anja Weise, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
International Journal of Oncology|June 7, 2003
Highly complex karyotypic changes in acute myelogenous leukemia: a case reportAnita Heller, Nikolai Rubtsov, Soili Kytölä, et al.
Molecular Cytogenetics|June 2, 2009
Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cellsJörn Erlecke, Isabell Hartmann, Martin Hoffmann, et al.
European Journal of Pediatrics|June 24, 2003
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literatureJörg Seidel, Anita Heller, Gabriele Senger, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
Karyotyping of human synaptonemal complexes by cenM-FISHMaria Oliver-Bonet, Thomas Liehr, Angela Nietzel, et al.
European Journal of Medical Genetics|September 24, 2005
Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotypeJoris Robert Vermeesch, Cindy Melotte, Ivo Salden, et al.
Journal of the Association of Genetic Technologists|June 24, 2004
Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic ApproachesThomas Liehr, Angela Nietzel, Heike Starke, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangementsHeike Starke, Jörg Seidel, Wolfram Henn, et al.
Clinical Dysmorphology|September 13, 2005
Three new cases with a supernumerary ring chromosome 1Laura Rodríguez, Heike Starke, Nieves Martínez Guardia, et al.
Human Genetics|September 19, 2003
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classificationHeike Starke, Angela Nietzel, Anja Weise, et al.
Pageof 4