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Acta Paediatrica Scandinavica
|
September 1, 1989
The effect of caffeine compared with theophylline in the treatment of idiopathic apnea in premature infants
G Fuglsang, K Nielsen, L Kjaer Nielsen, et al.
Ugeskrift for Laeger
|
September 15, 1980
[Mucocutaneous lymph node syndrome, Kawasaki disease. A review and report of 3 cases]
N H Rasmussen, I L Pedersen, T Thelle, et al.
Annales De Genetique
|
January 1, 1982
Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1
P K Jensen, C Junien, S Despoisse, et al.
Journal of Musculoskeletal & Neuronal Interactions
|
June 3, 2017
Muscular response to the first three months of deflazacort treatment in boys with Duchenne muscular dystrophy
L Jensen, S J Petersson, N O Illum, et al.
Journal of Inherited Metabolic Disease
|
June 12, 2009
Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency
E Ostergaard, L Birk Moller, H Serap Kalkanoglu-Sivri, et al.
Ugeskrift for Laeger
|
April 2, 1979
[Measurement of testicular volume with Prader's orchiometer in 1,389 boys 5--15 1/2 years old]
K Sørensen, J Nielsen, P Busch, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2010
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene
A Orrico, L Galli, L Faivre, et al.
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of 2
Search research articles
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Showing results (11-20 of 17) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 17 results.
Acta Paediatrica Scandinavica
|
September 1, 1989
The effect of caffeine compared with theophylline in the treatment of idiopathic apnea in premature infants
G Fuglsang, K Nielsen, L Kjaer Nielsen, et al.
Ugeskrift for Laeger
|
September 15, 1980
[Mucocutaneous lymph node syndrome, Kawasaki disease. A review and report of 3 cases]
N H Rasmussen, I L Pedersen, T Thelle, et al.
Annales De Genetique
|
January 1, 1982
Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1
P K Jensen, C Junien, S Despoisse, et al.
Journal of Musculoskeletal & Neuronal Interactions
|
June 3, 2017
Muscular response to the first three months of deflazacort treatment in boys with Duchenne muscular dystrophy
L Jensen, S J Petersson, N O Illum, et al.
Journal of Inherited Metabolic Disease
|
June 12, 2009
Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency
E Ostergaard, L Birk Moller, H Serap Kalkanoglu-Sivri, et al.
Ugeskrift for Laeger
|
April 2, 1979
[Measurement of testicular volume with Prader's orchiometer in 1,389 boys 5--15 1/2 years old]
K Sørensen, J Nielsen, P Busch, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2010
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene
A Orrico, L Galli, L Faivre, et al.
Page
of 2