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H R WIEDEMANN

Showing results (121-130 of 151) with videos related to

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Humangenetik|August 25, 1975
The tetraphocomelia -- cleft palate syndrome: description of a new caseF R Grosse, C Pandel, H R Wiedemann
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1971
[On achondrogenesis (author's transl)]W Remagen, H A Hienz, H R Wiedemann
American Journal of Medical Genetics|March 1, 1990
Previously unrecognized congenital progeroid disorderE M Petty, R Laxova, H R Wiedemann
Die Medizinische Welt|November 13, 1981
[Procedure in congenital total virilization of the external genitalia (pseudohermaphroditismus femininus)]K von Schnakenburg, K Kruse, H R Wiedemann
Die Medizinische Welt|June 5, 1981
[Disease spectrum in oligosymptomatic hypothyroidism]H D Oldigs, K von Schnakenburg, H R Wiedemann
Deutsche Medizinische Wochenschrift (1946)|December 1, 1972
[Treatment of progressive fibrodysplasia ossificans with diphosphonate (EHDP)]K von Schnakenburg, G Gross-Selbeck, H R Wiedemann
European Journal of Pediatrics|December 1, 1984
Prenatal diagnosis of a probable hereditary syndrome with holoprosencephaly, hydrocephaly, octodactyly, and cardiac malformationsW Grote, H Rehder, D Weisner, et al.
Clinical Genetics|January 1, 1989
Growth, bone maturation and pubertal development in children with the EMG-syndromeW G Sippell, C J Partsch, H R Wiedemann
European Journal of Pediatrics|July 1, 1981
Dysplasia epiphysealis hemimelica--Trevor disease. Severe manifestations in a childH R Wiedemann, M Mann, P S von Kreudenstein
Klinische Padiatrie|November 1, 1978
[Monophylic vacuolisation of promyelocytes in Menke's-syndrome (trichopoliodystrophy) (author's transl)]K Heyne, K Dörner, E Graucob, et al.
Pageof 16

Showing results (121-130 of 151) with videos related to

Sort By:
Pageof 16
Humangenetik|August 25, 1975
The tetraphocomelia -- cleft palate syndrome: description of a new caseF R Grosse, C Pandel, H R Wiedemann
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1971
[On achondrogenesis (author's transl)]W Remagen, H A Hienz, H R Wiedemann
American Journal of Medical Genetics|March 1, 1990
Previously unrecognized congenital progeroid disorderE M Petty, R Laxova, H R Wiedemann
Die Medizinische Welt|November 13, 1981
[Procedure in congenital total virilization of the external genitalia (pseudohermaphroditismus femininus)]K von Schnakenburg, K Kruse, H R Wiedemann
Die Medizinische Welt|June 5, 1981
[Disease spectrum in oligosymptomatic hypothyroidism]H D Oldigs, K von Schnakenburg, H R Wiedemann
Deutsche Medizinische Wochenschrift (1946)|December 1, 1972
[Treatment of progressive fibrodysplasia ossificans with diphosphonate (EHDP)]K von Schnakenburg, G Gross-Selbeck, H R Wiedemann
European Journal of Pediatrics|December 1, 1984
Prenatal diagnosis of a probable hereditary syndrome with holoprosencephaly, hydrocephaly, octodactyly, and cardiac malformationsW Grote, H Rehder, D Weisner, et al.
Clinical Genetics|January 1, 1989
Growth, bone maturation and pubertal development in children with the EMG-syndromeW G Sippell, C J Partsch, H R Wiedemann
European Journal of Pediatrics|July 1, 1981
Dysplasia epiphysealis hemimelica--Trevor disease. Severe manifestations in a childH R Wiedemann, M Mann, P S von Kreudenstein
Klinische Padiatrie|November 1, 1978
[Monophylic vacuolisation of promyelocytes in Menke's-syndrome (trichopoliodystrophy) (author's transl)]K Heyne, K Dörner, E Graucob, et al.
Pageof 16