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European Journal of Pediatrics
|
September 1, 1983
Dysplasia epiphysealis capitis femoris? A longitudinal observation
L Emmery, J Timmermans, J G Leroy
Acta Paediatrica Belgica
|
January 1, 1971
Brain damage as a consequence of unrecognised hypohidrotic ectodermal dysplasia
J Jaeken, L Emmery, M Casteels-van Daele
Acta Paediatrica Belgica
|
January 1, 1970
[Spontaneous perforation of the small intestine in the newborn]
L Emmery, R Kerremans, V Desmet, et al.
European Journal of Pediatrics
|
October 1, 1983
Familial infantile cortical hyperostosis
L Emmery, J Timmermans, J Christens, et al.
Annales De Genetique
|
January 1, 1981
Pierre-Robin anomalad, moderate mental retardation and distal 4q deletion
J P Fryns, J Timmermans, J Hoedemaekers, et al.
Archives of Disease in Childhood
|
February 1, 1978
Defective neutrophil chemotaxis and raised serum ige levels in a child with recurrent bacterial infections and eczema. Influence of levamisole
J De Cree, L Emmery, J Timmermans, et al.
Journal De Genetique Humaine
|
March 1, 1980
Tricho-rhino-phalangeal syndrome type II: Langer-Giedion syndrome in a 2.5 years-old boy
J P Fryns, L Emmery, J Timmermans, et al.
Human Genetics
|
October 1, 1979
Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers
M Boel, J Timmermans, L Emmery, et al.
Acta Paediatrica Belgica
|
April 1, 1979
The Wolf-Hirschhorn syndrome. Deletion of the short arm of chromosome 4
J P Fryns, B François, J Timmermans, et al.
Human Genetics
|
September 2, 1979
Ring chromosome 15 syndrome
J P Fryns, J Timmermans, F D Hondt, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
European Journal of Pediatrics
|
September 1, 1983
Dysplasia epiphysealis capitis femoris? A longitudinal observation
L Emmery, J Timmermans, J G Leroy
Acta Paediatrica Belgica
|
January 1, 1971
Brain damage as a consequence of unrecognised hypohidrotic ectodermal dysplasia
J Jaeken, L Emmery, M Casteels-van Daele
Acta Paediatrica Belgica
|
January 1, 1970
[Spontaneous perforation of the small intestine in the newborn]
L Emmery, R Kerremans, V Desmet, et al.
European Journal of Pediatrics
|
October 1, 1983
Familial infantile cortical hyperostosis
L Emmery, J Timmermans, J Christens, et al.
Annales De Genetique
|
January 1, 1981
Pierre-Robin anomalad, moderate mental retardation and distal 4q deletion
J P Fryns, J Timmermans, J Hoedemaekers, et al.
Archives of Disease in Childhood
|
February 1, 1978
Defective neutrophil chemotaxis and raised serum ige levels in a child with recurrent bacterial infections and eczema. Influence of levamisole
J De Cree, L Emmery, J Timmermans, et al.
Journal De Genetique Humaine
|
March 1, 1980
Tricho-rhino-phalangeal syndrome type II: Langer-Giedion syndrome in a 2.5 years-old boy
J P Fryns, L Emmery, J Timmermans, et al.
Human Genetics
|
October 1, 1979
Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers
M Boel, J Timmermans, L Emmery, et al.
Acta Paediatrica Belgica
|
April 1, 1979
The Wolf-Hirschhorn syndrome. Deletion of the short arm of chromosome 4
J P Fryns, B François, J Timmermans, et al.
Human Genetics
|
September 2, 1979
Ring chromosome 15 syndrome
J P Fryns, J Timmermans, F D Hondt, et al.
Page
of 2