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

G Schwanitz

Showing results (61-70 of 123) with videos related to

Pageof 13
Sort By:
Deutsche Medizinische Wochenschrift (1946)|February 10, 1999
[Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2]D Trost, H Engels, G Bauriedel, et al.
Humangenetik|January 1, 1971
[Mosaic of G-G translocation observed in a girl with faint symptoms of mongolism]K P Grosse, G Schwanitz, G Grosse, et al.
Blut|December 1, 1971
[Congenital dyserythropoietic anemia]G Hartwich, F Wolf, J Becker, et al.
Journal De Genetique Humaine|June 1, 1977
[Familial translocation 3/22 MAT with partial trisomy 3q (author's transl)]G Schwanitz, R D Schmid, G Grosse, et al.
Human Genetics|December 1, 1989
Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colliG Schwanitz, K Zerres, U Gembruch, et al.
Journal of Medical Genetics|August 6, 2000
Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2D Trost, W Wiebe, S Uhlhaas, et al.
Advances in Medical Sciences|July 11, 2008
Abnormalities in tooth morphology, structure and dentition in two children with chromosome aberrations. Translocation trisomy 13 and trisomy 21A Roos, T Eggermann, S Zschiesche, et al.
Annales De Genetique|January 1, 1989
Duplication 7p de novo and literature reviewK Zerres, G Schwanitz, K Gellissen, et al.
American Journal of Medical Genetics|September 19, 1997
Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selectionR Schubert, R Viersbach, T Eggermann, et al.
Humangenetik|January 1, 1972
C 11-D 13-translocation in four generationsH D Rott, G Schwanitz, K P Grosse, et al.
Pageof 13

Showing results (61-70 of 123) with videos related to

Sort By:
Pageof 13
Deutsche Medizinische Wochenschrift (1946)|February 10, 1999
[Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2]D Trost, H Engels, G Bauriedel, et al.
Humangenetik|January 1, 1971
[Mosaic of G-G translocation observed in a girl with faint symptoms of mongolism]K P Grosse, G Schwanitz, G Grosse, et al.
Blut|December 1, 1971
[Congenital dyserythropoietic anemia]G Hartwich, F Wolf, J Becker, et al.
Journal De Genetique Humaine|June 1, 1977
[Familial translocation 3/22 MAT with partial trisomy 3q (author's transl)]G Schwanitz, R D Schmid, G Grosse, et al.
Human Genetics|December 1, 1989
Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colliG Schwanitz, K Zerres, U Gembruch, et al.
Journal of Medical Genetics|August 6, 2000
Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2D Trost, W Wiebe, S Uhlhaas, et al.
Advances in Medical Sciences|July 11, 2008
Abnormalities in tooth morphology, structure and dentition in two children with chromosome aberrations. Translocation trisomy 13 and trisomy 21A Roos, T Eggermann, S Zschiesche, et al.
Annales De Genetique|January 1, 1989
Duplication 7p de novo and literature reviewK Zerres, G Schwanitz, K Gellissen, et al.
American Journal of Medical Genetics|September 19, 1997
Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selectionR Schubert, R Viersbach, T Eggermann, et al.
Humangenetik|January 1, 1972
C 11-D 13-translocation in four generationsH D Rott, G Schwanitz, K P Grosse, et al.
Pageof 13