Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Heike Starke

Showing results (21-30 of 39) with videos related to

Pageof 4
Sort By:
Human Molecular Genetics|September 13, 2005
Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human malesFei Sun, Maria Oliver-Bonet, Thomas Liehr, et al.
International Journal of Molecular Medicine|March 14, 2002
Microdissection based high resolution multicolor banding for all 24 human chromosomesThomas Liehr, Anita Heller, Heike Starke, et al.
Prenatal Diagnosis|June 5, 2007
A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriersIna Fickelscher, Heike Starke, Eberhard Schulze, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16Heike Starke, Beate Mitulla, Angela Nietzel, et al.
Prenatal Diagnosis|September 17, 2003
First postnatal case of mosaic del(22)/r(22)Heike Starke, Beate Mitulla, Volkmar Beensen, et al.
Prenatal Diagnosis|July 13, 2002
Two more possible pitfalls of rapid prenatal diagnostics using interphase nucleiThomas Liehr, Isolde Schreyer, Annett Neumann, et al.
American Journal of Human Genetics|February 20, 2004
Human male recombination maps for individual chromosomesFei Sun, Maria Oliver-Bonet, Thomas Liehr, et al.
American Journal of Medical Genetics. Part A|April 4, 2003
Ten years follow up of a boy with a complex chromosomal rearrangement: going from a > 5 to 15-breakpoint CCRGunnar Houge, Thomas Liehr, Jacqueline Schoumans, et al.
Genes, Chromosomes & Cancer|April 30, 2002
Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemiaIvan F Loncarevic, Jennifer Römer, Heike Starke, et al.
Prenatal Diagnosis|May 16, 2003
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pterVladimir Trifonov, Jörg Seidel, Heike Starke, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|September 13, 2005
Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human malesFei Sun, Maria Oliver-Bonet, Thomas Liehr, et al.
International Journal of Molecular Medicine|March 14, 2002
Microdissection based high resolution multicolor banding for all 24 human chromosomesThomas Liehr, Anita Heller, Heike Starke, et al.
Prenatal Diagnosis|June 5, 2007
A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriersIna Fickelscher, Heike Starke, Eberhard Schulze, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16Heike Starke, Beate Mitulla, Angela Nietzel, et al.
Prenatal Diagnosis|September 17, 2003
First postnatal case of mosaic del(22)/r(22)Heike Starke, Beate Mitulla, Volkmar Beensen, et al.
Prenatal Diagnosis|July 13, 2002
Two more possible pitfalls of rapid prenatal diagnostics using interphase nucleiThomas Liehr, Isolde Schreyer, Annett Neumann, et al.
American Journal of Human Genetics|February 20, 2004
Human male recombination maps for individual chromosomesFei Sun, Maria Oliver-Bonet, Thomas Liehr, et al.
American Journal of Medical Genetics. Part A|April 4, 2003
Ten years follow up of a boy with a complex chromosomal rearrangement: going from a > 5 to 15-breakpoint CCRGunnar Houge, Thomas Liehr, Jacqueline Schoumans, et al.
Genes, Chromosomes & Cancer|April 30, 2002
Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemiaIvan F Loncarevic, Jennifer Römer, Heike Starke, et al.
Prenatal Diagnosis|May 16, 2003
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pterVladimir Trifonov, Jörg Seidel, Heike Starke, et al.
Pageof 4