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

H Starke

Showing results (51-60 of 74) with videos related to

Pageof 8
Sort By:
European Journal of Human Genetics : EJHG|August 31, 2001
Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated markerA Dufke, C Walczak, T Liehr, et al.
Prenatal Diagnosis|December 11, 1999
Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8H Starke, I Schreyer, C Kähler, et al.
Cytogenetic and Genome Research|March 9, 2004
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding methodA Weise, A Heller, H Starke, et al.
American Journal of Medical Genetics|August 3, 2001
Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expressionP Stankiewicz, H Thiele, I Giannakudis, et al.
Cytogenetic and Genome Research|November 20, 2002
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA librariesT Liehr, A Weise, A Heller, et al.
Human Reproduction (Oxford, England)|June 6, 2006
Analysis of non-crossover bivalents in pachytene cells from 10 normal menFei Sun, M Oliver-Bonet, T Liehr, et al.
Cytogenetic and Genome Research|February 24, 2007
Array painting using microdissected chromosomes to map chromosomal breakpointsL Backx, H Van Esch, C Melotte, et al.
American Journal of Medical Genetics. Part A|July 12, 2005
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delayG von Beust, S M Sauter, T Liehr, et al.
Journal of Medical Genetics|July 13, 2002
Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11-->q11:)/46,XX karyotypeF Von Eggeling, C Hoppe, U Bartz, et al.
Journal of Medical Genetics|June 19, 2002
Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probesA Weise, H Starke, A Heller, et al.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
European Journal of Human Genetics : EJHG|August 31, 2001
Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated markerA Dufke, C Walczak, T Liehr, et al.
Prenatal Diagnosis|December 11, 1999
Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8H Starke, I Schreyer, C Kähler, et al.
Cytogenetic and Genome Research|March 9, 2004
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding methodA Weise, A Heller, H Starke, et al.
American Journal of Medical Genetics|August 3, 2001
Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expressionP Stankiewicz, H Thiele, I Giannakudis, et al.
Cytogenetic and Genome Research|November 20, 2002
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA librariesT Liehr, A Weise, A Heller, et al.
Human Reproduction (Oxford, England)|June 6, 2006
Analysis of non-crossover bivalents in pachytene cells from 10 normal menFei Sun, M Oliver-Bonet, T Liehr, et al.
Cytogenetic and Genome Research|February 24, 2007
Array painting using microdissected chromosomes to map chromosomal breakpointsL Backx, H Van Esch, C Melotte, et al.
American Journal of Medical Genetics. Part A|July 12, 2005
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delayG von Beust, S M Sauter, T Liehr, et al.
Journal of Medical Genetics|July 13, 2002
Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11-->q11:)/46,XX karyotypeF Von Eggeling, C Hoppe, U Bartz, et al.
Journal of Medical Genetics|June 19, 2002
Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probesA Weise, H Starke, A Heller, et al.
Pageof 8