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

E Schwinger

Showing results (41-50 of 213) with videos related to

Pageof 22
Sort By:
Human Genetics|December 15, 1976
Studies on frequency of Y chromatin in human spermE Schwinger, J Ites, B Korte
Clinical Genetics|September 1, 1978
Sex determination in nuclei of amnion fluid cellsE Schwinger, D Klimmeck, M Hansmann
Deutsche Medizinische Wochenschrift (1946)|January 23, 1970
[Testicular function in men with XYY chromosomes. Meiosis and morphological findings]U Tettenborn, E Schwinger, A Gropp
Human Heredity|January 1, 1987
Four DNA polymorphisms on the short arm of the X chromosome: allele frequencies in a German and in a Turkish populationM Schürmann, R Warneke, E Schwinger
Zeitschrift Fur Kinderheilkunde|January 1, 1971
[Studies on patients with Down's syndrome. 3. Fluorescence microscopy studies]E Schwinger, H Roers, C Rittner
Acta Neurologica Scandinavica|March 10, 2001
Limited somatic mosaicism for Friedreich's ataxia GAA triplet repeat expansions identified by small pool PCR in blood leukocytesY Hellenbroich, E Schwinger, C Zühlke
Human Genetics|August 1, 1996
Analysis of sex and delta F508 in single amniocytes using primer extension preamplificationF Schaaff, H Wedemann, E Schwinger
Clinical Dysmorphology|July 1, 1992
Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritanceA Artlich, E Schwinger, P Meinecke
Fortschritte Der Neurologie-Psychiatrie|April 1, 1985
[Sporadic and familial-occurring multiple sclerosis. HLA typing and study of chromosomal sister chromatid exchange rate]J M Träder, K Warecka, E Schwinger
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1988
[Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract]K Heyne, Y S Shin, E Schwinger
Pageof 22

Showing results (41-50 of 213) with videos related to

Sort By:
Pageof 22
Human Genetics|December 15, 1976
Studies on frequency of Y chromatin in human spermE Schwinger, J Ites, B Korte
Clinical Genetics|September 1, 1978
Sex determination in nuclei of amnion fluid cellsE Schwinger, D Klimmeck, M Hansmann
Deutsche Medizinische Wochenschrift (1946)|January 23, 1970
[Testicular function in men with XYY chromosomes. Meiosis and morphological findings]U Tettenborn, E Schwinger, A Gropp
Human Heredity|January 1, 1987
Four DNA polymorphisms on the short arm of the X chromosome: allele frequencies in a German and in a Turkish populationM Schürmann, R Warneke, E Schwinger
Zeitschrift Fur Kinderheilkunde|January 1, 1971
[Studies on patients with Down's syndrome. 3. Fluorescence microscopy studies]E Schwinger, H Roers, C Rittner
Acta Neurologica Scandinavica|March 10, 2001
Limited somatic mosaicism for Friedreich's ataxia GAA triplet repeat expansions identified by small pool PCR in blood leukocytesY Hellenbroich, E Schwinger, C Zühlke
Human Genetics|August 1, 1996
Analysis of sex and delta F508 in single amniocytes using primer extension preamplificationF Schaaff, H Wedemann, E Schwinger
Clinical Dysmorphology|July 1, 1992
Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritanceA Artlich, E Schwinger, P Meinecke
Fortschritte Der Neurologie-Psychiatrie|April 1, 1985
[Sporadic and familial-occurring multiple sclerosis. HLA typing and study of chromosomal sister chromatid exchange rate]J M Träder, K Warecka, E Schwinger
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1988
[Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract]K Heyne, Y S Shin, E Schwinger
Pageof 22