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

H R WIEDEMANN

Showing results (131-140 of 151) with videos related to

Pageof 16
Sort By:
American Journal of Medical Genetics|December 30, 1996
Unusual complex of ventral midline anomalies: a multiple congenital anomalies/mental retardation syndromeA Bohring, J Sonntag, H Schröder, et al.
Monatsschrift Fur Kinderheilkunde|July 1, 1973
[Use of desensitization in childhood phobias]G Gutezeit, H R Wiedemann, K Aissen, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|May 1, 1974
Unusual glycolipids in brain cortex of a visceral lipidosis (Niemann-Pick disease?)R Kannan, H B Tjiong, H Debuch, et al.
American Journal of Medical Genetics|February 1, 1990
Proteus syndrome: course of a severe caseA Malamitsi-Puchner, D Dimitriadis, C Bartsocas, et al.
Archiv Fur Kinderheilkunde|January 1, 1970
[Symptomatology of the ring chromosomes of the D group. (2 new observations of type 13r)]M Tolksdorf, U Goll, H R Wiedemann, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|February 1, 1971
[Augmentation of bis(monoacylglycerin)phosphric acid in sphingomyelinosis (M. Niemann-Pick?)]P N Seng, H Debuch, B Witter, et al.
The Journal of Bone and Joint Surgery. British Volume|January 1, 1982
Systemic lipomatosis of bone. A case reportR Döhler, H L Poser, D Harms, et al.
American Journal of Medical Genetics|June 1, 1993
Hirsutism-skeletal dysplasia-mental retardation syndrome with abnormal face and a uric acid metabolism disorderH R Wiedemann, H D Oldigs, H C Oppermann, et al.
European Journal of Pediatrics|March 1, 1983
Prenatal diagnosis of a short-rib-polydactylia syndrome type Saldino-Noonan at 17 weeks' gestationW Grote, D Weisner, U Jänig, et al.
Klinische Padiatrie|November 1, 1975
[Congenital spondylo-epiphyseal dysplasia: follow-up of a case over 9 years (author's transl)]T Luthardt, H Reinwein, H Schönenberg, et al.
Pageof 16

Showing results (131-140 of 151) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics|December 30, 1996
Unusual complex of ventral midline anomalies: a multiple congenital anomalies/mental retardation syndromeA Bohring, J Sonntag, H Schröder, et al.
Monatsschrift Fur Kinderheilkunde|July 1, 1973
[Use of desensitization in childhood phobias]G Gutezeit, H R Wiedemann, K Aissen, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|May 1, 1974
Unusual glycolipids in brain cortex of a visceral lipidosis (Niemann-Pick disease?)R Kannan, H B Tjiong, H Debuch, et al.
American Journal of Medical Genetics|February 1, 1990
Proteus syndrome: course of a severe caseA Malamitsi-Puchner, D Dimitriadis, C Bartsocas, et al.
Archiv Fur Kinderheilkunde|January 1, 1970
[Symptomatology of the ring chromosomes of the D group. (2 new observations of type 13r)]M Tolksdorf, U Goll, H R Wiedemann, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|February 1, 1971
[Augmentation of bis(monoacylglycerin)phosphric acid in sphingomyelinosis (M. Niemann-Pick?)]P N Seng, H Debuch, B Witter, et al.
The Journal of Bone and Joint Surgery. British Volume|January 1, 1982
Systemic lipomatosis of bone. A case reportR Döhler, H L Poser, D Harms, et al.
American Journal of Medical Genetics|June 1, 1993
Hirsutism-skeletal dysplasia-mental retardation syndrome with abnormal face and a uric acid metabolism disorderH R Wiedemann, H D Oldigs, H C Oppermann, et al.
European Journal of Pediatrics|March 1, 1983
Prenatal diagnosis of a short-rib-polydactylia syndrome type Saldino-Noonan at 17 weeks' gestationW Grote, D Weisner, U Jänig, et al.
Klinische Padiatrie|November 1, 1975
[Congenital spondylo-epiphyseal dysplasia: follow-up of a case over 9 years (author's transl)]T Luthardt, H Reinwein, H Schönenberg, et al.
Pageof 16