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Humangenetik
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August 25, 1975
The tetraphocomelia -- cleft palate syndrome: description of a new case
F 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 disorder
E 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 malformations
W Grote, H Rehder, D Weisner, et al.
Clinical Genetics
|
January 1, 1989
Growth, bone maturation and pubertal development in children with the EMG-syndrome
W G Sippell, C J Partsch, H R Wiedemann
European Journal of Pediatrics
|
July 1, 1981
Dysplasia epiphysealis hemimelica--Trevor disease. Severe manifestations in a child
H 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.
Page
of 16
Search research articles
Search
Showing results (121-130 of 151) with videos related to
Sort By:
Page
of 16
Humangenetik
|
August 25, 1975
The tetraphocomelia -- cleft palate syndrome: description of a new case
F 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 disorder
E 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 malformations
W Grote, H Rehder, D Weisner, et al.
Clinical Genetics
|
January 1, 1989
Growth, bone maturation and pubertal development in children with the EMG-syndrome
W G Sippell, C J Partsch, H R Wiedemann
European Journal of Pediatrics
|
July 1, 1981
Dysplasia epiphysealis hemimelica--Trevor disease. Severe manifestations in a child
H 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.
Page
of 16