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 (21-30 of 205) with videos related to

Pageof 21
Sort By:
Annales De Genetique|January 1, 1993
Tandem duplication 11q23-ter in the dysmorphic child of a retarded mother mosaic for the same anomaly with no apparent abnormalitiesR A Pfeiffer, C Schütz
Journal of Neurology|July 20, 1977
[Hypoplasia ponto-neocerebellaris (author's transl)]J Peiffer, R A Pfeiffer
Humangenetik|January 1, 1975
The phocomelia-thrombocytopenia syndrome. A follow-up reportR A Pfeiffer, C Haneke
American Journal of Medical Genetics|November 15, 1993
Hemimelia in Brachmann-de Lange syndrome (BDLS): a patient with severe deficiency of the upper and lower limbsR A Pfeiffer, J Correll
Human Genetics|January 1, 1982
Mirror image duplications of chromosome 21. Three new cases and discussion of the mechanisms of originR A Pfeiffer, J Loidl
Klinische Padiatrie|March 1, 1975
[Is there a syndrome of Ullrich and Feichtiger?(Author's transl)]R A Pfeiffer, H Slavaykoff
Journal of Medical Genetics|October 1, 1982
Congenital universal alopecia, mental deficiency, and microcephaly in two sibsR A Pfeiffer, J Völklein
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1984
[Phenotype of trisomy 9]R A Pfeiffer, R Müller
Ophthalmic Paediatrics and Genetics|April 1, 1985
Familial congenital cataract, non-progressive neurological disorders and mental deficiency: a new X-linked syndrome?R A Pfeiffer, J Steffann
Monatsschrift Fur Kinderheilkunde|July 1, 1971
[Forms of intersexuality in X0-XY-mosaicism]H Stolecke, R A Pfeiffer
Pageof 21

Showing results (21-30 of 205) with videos related to

Sort By:
Pageof 21
Annales De Genetique|January 1, 1993
Tandem duplication 11q23-ter in the dysmorphic child of a retarded mother mosaic for the same anomaly with no apparent abnormalitiesR A Pfeiffer, C Schütz
Journal of Neurology|July 20, 1977
[Hypoplasia ponto-neocerebellaris (author's transl)]J Peiffer, R A Pfeiffer
Humangenetik|January 1, 1975
The phocomelia-thrombocytopenia syndrome. A follow-up reportR A Pfeiffer, C Haneke
American Journal of Medical Genetics|November 15, 1993
Hemimelia in Brachmann-de Lange syndrome (BDLS): a patient with severe deficiency of the upper and lower limbsR A Pfeiffer, J Correll
Human Genetics|January 1, 1982
Mirror image duplications of chromosome 21. Three new cases and discussion of the mechanisms of originR A Pfeiffer, J Loidl
Klinische Padiatrie|March 1, 1975
[Is there a syndrome of Ullrich and Feichtiger?(Author's transl)]R A Pfeiffer, H Slavaykoff
Journal of Medical Genetics|October 1, 1982
Congenital universal alopecia, mental deficiency, and microcephaly in two sibsR A Pfeiffer, J Völklein
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1984
[Phenotype of trisomy 9]R A Pfeiffer, R Müller
Ophthalmic Paediatrics and Genetics|April 1, 1985
Familial congenital cataract, non-progressive neurological disorders and mental deficiency: a new X-linked syndrome?R A Pfeiffer, J Steffann
Monatsschrift Fur Kinderheilkunde|July 1, 1971
[Forms of intersexuality in X0-XY-mosaicism]H Stolecke, R A Pfeiffer
Pageof 21