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

T Haaf

Showing results (131-140 of 170) with videos related to

Pageof 17
Sort By:
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 5, 2011
Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile malesN El Hajj, U Zechner, E Schneider, et al.
Journal of Thrombosis and Haemostasis : JTH|July 2, 2013
Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNAB Pezeshkpoor, N Zimmer, N Marquardt, et al.
Cytogenetic and Genome Research|November 17, 2004
Genomic structure and paralogous regions of the inversion breakpoint occurring between human chromosome 3p12.3 and orangutan chromosome 2Y Yue, B Grossmann, E Tsend-Ayush, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 9, 1999
Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease?K Stout, S van der Maarel, R R Frants, et al.
Cytogenetics and Cell Genetics|August 31, 2001
Chicken microchromosomes are hypermethylated and can be identified by specific painting probesF Grützner, E Zend-Ajusch, K Stout, et al.
Journal of Medical Genetics|May 24, 2005
Disruption of TCBA1 associated with a de novo t(1;6)(q32.2;q22.3) presenting in a child with developmental delay and recurrent infectionsY Yue, K Stout, B Grossmann, et al.
Cytogenetics and Cell Genetics|February 22, 2002
Comparative mapping of the human 9q34 region in Fugu rubripesN Bouchireb, F Grützner, T Haaf, et al.
Cytogenetic and Genome Research|November 20, 2002
Chromosome banding in Amphibia. XXII. Atypical y chromosomes in Gastrotheca walkeri and Gastrotheca ovifera (Anura, Hylidae)M Schmid, W Feichtinger, C Steinlein, et al.
Cytogenetic and Genome Research|September 10, 2009
Haploinsufficiency of 16.4 Mb from chromosome 22pter-q11.21 in a girl with unilateral conductive hearing lossN Damatova, V Beyer, D Galetzka, et al.
Molecular Syndromology|February 20, 2014
A Boy with an LCR3/4-Flanked 10q22.3q23.2 Microdeletion and Uncommon Phenotypic FeaturesE Petrova, C Neuner, T Haaf, et al.
Pageof 17

Showing results (131-140 of 170) with videos related to

Sort By:
Pageof 17
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 5, 2011
Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile malesN El Hajj, U Zechner, E Schneider, et al.
Journal of Thrombosis and Haemostasis : JTH|July 2, 2013
Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNAB Pezeshkpoor, N Zimmer, N Marquardt, et al.
Cytogenetic and Genome Research|November 17, 2004
Genomic structure and paralogous regions of the inversion breakpoint occurring between human chromosome 3p12.3 and orangutan chromosome 2Y Yue, B Grossmann, E Tsend-Ayush, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 9, 1999
Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease?K Stout, S van der Maarel, R R Frants, et al.
Cytogenetics and Cell Genetics|August 31, 2001
Chicken microchromosomes are hypermethylated and can be identified by specific painting probesF Grützner, E Zend-Ajusch, K Stout, et al.
Journal of Medical Genetics|May 24, 2005
Disruption of TCBA1 associated with a de novo t(1;6)(q32.2;q22.3) presenting in a child with developmental delay and recurrent infectionsY Yue, K Stout, B Grossmann, et al.
Cytogenetics and Cell Genetics|February 22, 2002
Comparative mapping of the human 9q34 region in Fugu rubripesN Bouchireb, F Grützner, T Haaf, et al.
Cytogenetic and Genome Research|November 20, 2002
Chromosome banding in Amphibia. XXII. Atypical y chromosomes in Gastrotheca walkeri and Gastrotheca ovifera (Anura, Hylidae)M Schmid, W Feichtinger, C Steinlein, et al.
Cytogenetic and Genome Research|September 10, 2009
Haploinsufficiency of 16.4 Mb from chromosome 22pter-q11.21 in a girl with unilateral conductive hearing lossN Damatova, V Beyer, D Galetzka, et al.
Molecular Syndromology|February 20, 2014
A Boy with an LCR3/4-Flanked 10q22.3q23.2 Microdeletion and Uncommon Phenotypic FeaturesE Petrova, C Neuner, T Haaf, et al.
Pageof 17