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

A Jauch

Showing results (71-80 of 109) with videos related to

Pageof 11
Sort By:
Human Genetics|March 1, 1997
High-resolution comparative hybridization to combed DNA fibersJ Kraus, R G Weber, M Cremer, et al.
American Journal of Medical Genetics|August 22, 2000
Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generationsF Speleman, B Callens, K Logghe, et al.
Clinical Genetics|August 5, 2010
Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?C Evers, P H Heidemann, D Dunstheimer, et al.
Human Genetics|September 12, 2000
Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individualsM Granzow, S Popp, M Keller, et al.
Human Genetics|June 1, 1996
Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGHH J Decker, C Neuhaus, A Jauch, et al.
Clinical Genetics|April 26, 2013
Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1: further insights into a genetic paradoxC Evers, M S Jungwirth, J Morgenthaler, et al.
The American Journal of Pathology|June 1, 1994
Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and lossesE Schröck, G Thiel, T Lozanova, et al.
Human Molecular Genetics|May 1, 1993
Chromosomal bar codes produced by multicolor fluorescence in situ hybridization with multiple YAC clones and whole chromosome painting probesC Lengauer, M R Speicher, S Popp, et al.
Oncogene|July 6, 2001
Alternative lengthening of telomeres is associated with chromosomal instability in osteosarcomasC Scheel, K L Schaefer, A Jauch, et al.
Human Genetics|December 18, 1998
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversionW Courtens, D Grossman, N Van Roy, et al.
Pageof 11

Showing results (71-80 of 109) with videos related to

Sort By:
Pageof 11
Human Genetics|March 1, 1997
High-resolution comparative hybridization to combed DNA fibersJ Kraus, R G Weber, M Cremer, et al.
American Journal of Medical Genetics|August 22, 2000
Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generationsF Speleman, B Callens, K Logghe, et al.
Clinical Genetics|August 5, 2010
Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?C Evers, P H Heidemann, D Dunstheimer, et al.
Human Genetics|September 12, 2000
Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individualsM Granzow, S Popp, M Keller, et al.
Human Genetics|June 1, 1996
Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGHH J Decker, C Neuhaus, A Jauch, et al.
Clinical Genetics|April 26, 2013
Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1: further insights into a genetic paradoxC Evers, M S Jungwirth, J Morgenthaler, et al.
The American Journal of Pathology|June 1, 1994
Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and lossesE Schröck, G Thiel, T Lozanova, et al.
Human Molecular Genetics|May 1, 1993
Chromosomal bar codes produced by multicolor fluorescence in situ hybridization with multiple YAC clones and whole chromosome painting probesC Lengauer, M R Speicher, S Popp, et al.
Oncogene|July 6, 2001
Alternative lengthening of telomeres is associated with chromosomal instability in osteosarcomasC Scheel, K L Schaefer, A Jauch, et al.
Human Genetics|December 18, 1998
Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversionW Courtens, D Grossman, N Van Roy, et al.
Pageof 11