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Markus Stumm

Showing results (21-30 of 26) with videos related to

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Journal of the Chinese Medical Association : JCMA|May 12, 2010
Small supernumerary marker chromosomes 1 with a normal phenotypeThomas Liehr, Rolf-Dieter Wegner, Markus Stumm, 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.
International Journal of Cancer|June 9, 2004
Increased cancer risk of heterozygotes with NBS1 germline mutations in PolandJan Steffen, Raymonda Varon, Maria Mosor, et al.
Prenatal Diagnosis|November 14, 2013
Diagnostic accuracy of random massively parallel sequencing for non-invasive prenatal detection of common autosomal aneuploidies: a collaborative study in EuropeMarkus Stumm, Michael Entezami, Karsten Haug, et al.
Human Genetics|September 19, 2003
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classificationHeike Starke, Angela Nietzel, Anja Weise, et al.
Molecular Cytogenetics|April 4, 2013
Heteromorphic variants of chromosome 9Nadezda Kosyakova, Ani Grigorian, Thomas Liehr, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Journal of the Chinese Medical Association : JCMA|May 12, 2010
Small supernumerary marker chromosomes 1 with a normal phenotypeThomas Liehr, Rolf-Dieter Wegner, Markus Stumm, 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.
International Journal of Cancer|June 9, 2004
Increased cancer risk of heterozygotes with NBS1 germline mutations in PolandJan Steffen, Raymonda Varon, Maria Mosor, et al.
Prenatal Diagnosis|November 14, 2013
Diagnostic accuracy of random massively parallel sequencing for non-invasive prenatal detection of common autosomal aneuploidies: a collaborative study in EuropeMarkus Stumm, Michael Entezami, Karsten Haug, et al.
Human Genetics|September 19, 2003
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classificationHeike Starke, Angela Nietzel, Anja Weise, et al.
Molecular Cytogenetics|April 4, 2013
Heteromorphic variants of chromosome 9Nadezda Kosyakova, Ani Grigorian, Thomas Liehr, et al.
Pageof 3