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

R A Pfeiffer

Showing results (71-80 of 205) with videos related to

Pageof 21
Sort By:
Deutsche Medizinische Wochenschrift (1946)|August 23, 1991
[The Hajdu-Cheney syndrome. The basilar impression as a diagnostic sign]B Laudi, M Klinger, R A Pfeiffer
Clinical Genetics|August 1, 1992
Typical and partial cat eye syndrome: identification of the marker chromosome by FISHT Liehr, R A Pfeiffer, U Trautmann
Lancet (London, England)|July 11, 1970
Extra chromosome in "cat eye" syndromeR A Pfeiffer, K Heimann, E Heiming
Journal De Genetique Humaine|August 1, 1986
Pericentric inversions of the X chromosome. A new observation and review of the published casesR A Pfeiffer, M Kossakiewicz, C Baisch
Zeitschrift Fur Kinderheilkunde|January 1, 1970
[The popliteal pterygium syndrome. A dominant autosomal malformation syndrome]R A Pfeiffer, W Tünte, M Reinken
Humangenetik|January 1, 1973
Partial trisomy 14 following a balanced reciprocal translocation t(14q-;21q+)R A Pfeiffer, K Büttinghaus, H Struck
Humangenetik|January 1, 1973
Tetraphocomelia and neonatal amegakaryocytic thrombocytopeniaR A Pfeiffer, G Maintz, C Haneke
Klinische Wochenschrift|July 15, 1971
[Fluorescent microscopy detection of human Y-chromosome in interphase nuclei using acridine derivatives ("atebrin", "acranil")]F Majewski, L Bier, R A Pfeiffer
European Journal of Pediatrics|January 1, 1987
Sagittal craniostenosis, congenital heart disease, mental deficiency and various dysmorphies in two sibs--a "new" syndrome?R A Pfeiffer, H Singer, S Zschiesche
Annales De Genetique|January 1, 1992
Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3R A Pfeiffer, G Legat, U Trautmann
Pageof 21

Showing results (71-80 of 205) with videos related to

Sort By:
Pageof 21
Deutsche Medizinische Wochenschrift (1946)|August 23, 1991
[The Hajdu-Cheney syndrome. The basilar impression as a diagnostic sign]B Laudi, M Klinger, R A Pfeiffer
Clinical Genetics|August 1, 1992
Typical and partial cat eye syndrome: identification of the marker chromosome by FISHT Liehr, R A Pfeiffer, U Trautmann
Lancet (London, England)|July 11, 1970
Extra chromosome in "cat eye" syndromeR A Pfeiffer, K Heimann, E Heiming
Journal De Genetique Humaine|August 1, 1986
Pericentric inversions of the X chromosome. A new observation and review of the published casesR A Pfeiffer, M Kossakiewicz, C Baisch
Zeitschrift Fur Kinderheilkunde|January 1, 1970
[The popliteal pterygium syndrome. A dominant autosomal malformation syndrome]R A Pfeiffer, W Tünte, M Reinken
Humangenetik|January 1, 1973
Partial trisomy 14 following a balanced reciprocal translocation t(14q-;21q+)R A Pfeiffer, K Büttinghaus, H Struck
Humangenetik|January 1, 1973
Tetraphocomelia and neonatal amegakaryocytic thrombocytopeniaR A Pfeiffer, G Maintz, C Haneke
Klinische Wochenschrift|July 15, 1971
[Fluorescent microscopy detection of human Y-chromosome in interphase nuclei using acridine derivatives ("atebrin", "acranil")]F Majewski, L Bier, R A Pfeiffer
European Journal of Pediatrics|January 1, 1987
Sagittal craniostenosis, congenital heart disease, mental deficiency and various dysmorphies in two sibs--a "new" syndrome?R A Pfeiffer, H Singer, S Zschiesche
Annales De Genetique|January 1, 1992
Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3R A Pfeiffer, G Legat, U Trautmann
Pageof 21