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Journal of Medical Genetics
|
January 1, 1997
Carbohydrate deficient glycoprotein (CDG) syndrome type I
J Jaeken, G Matthijs, R Barone, et al.
Proteomics
|
October 30, 2001
Band 3 glycoprotein and glycophorin A from erythrocytes of children with congenital disorder of glycosylation type-Ia are underglycosylated
E Zdebska, M Musielak, J Jaeken, et al.
Journal of Inherited Metabolic Disease
|
June 28, 2006
Normal pregnancy outcome in L-2-hydroxyglutaric aciduria
A Jonckheere, D Carton, J Jaeken, et al.
Acta Paediatrica Belgica
|
January 1, 1977
The Poland syndrome
J Jaeken, G Fabry, J Mulier, et al.
European Journal of Pediatrics
|
February 14, 1998
3-year-old girl with rickets and hepatomegaly
W Proesmans, J Decoster, L Breysem, et al.
Lancet (London, England)
|
July 31, 1982
Transient neonatal hyperammonaemia and herpes simplex infection
J Jaeken, H Devlieger, P Casaer, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
January 1, 1986
Inborn errors of GABA metabolism
K M Gibson, W L Nyhan, J Jaeken
Acta Paediatrica Belgica
|
January 1, 1971
Brain damage as a consequence of unrecognised hypohidrotic ectodermal dysplasia
J Jaeken, L Emmery, M Casteels-van Daele
Clinical Dysmorphology
|
May 18, 1999
Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocation
T Lukusa, K Devriendt, J Jaeken, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 14, 1991
Reference values for free gamma-aminobutyric acid determined by ion-exchange chromatography and fluorescence detection in the cerebrospinal fluid of children
H A Carchon, J Jaeken, E Jansen, et al.
Page
of 26
Search research articles
Search
Showing results (51-60 of 257) with videos related to
Sort By:
Page
of 26
Journal of Medical Genetics
|
January 1, 1997
Carbohydrate deficient glycoprotein (CDG) syndrome type I
J Jaeken, G Matthijs, R Barone, et al.
Proteomics
|
October 30, 2001
Band 3 glycoprotein and glycophorin A from erythrocytes of children with congenital disorder of glycosylation type-Ia are underglycosylated
E Zdebska, M Musielak, J Jaeken, et al.
Journal of Inherited Metabolic Disease
|
June 28, 2006
Normal pregnancy outcome in L-2-hydroxyglutaric aciduria
A Jonckheere, D Carton, J Jaeken, et al.
Acta Paediatrica Belgica
|
January 1, 1977
The Poland syndrome
J Jaeken, G Fabry, J Mulier, et al.
European Journal of Pediatrics
|
February 14, 1998
3-year-old girl with rickets and hepatomegaly
W Proesmans, J Decoster, L Breysem, et al.
Lancet (London, England)
|
July 31, 1982
Transient neonatal hyperammonaemia and herpes simplex infection
J Jaeken, H Devlieger, P Casaer, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
January 1, 1986
Inborn errors of GABA metabolism
K M Gibson, W L Nyhan, J Jaeken
Acta Paediatrica Belgica
|
January 1, 1971
Brain damage as a consequence of unrecognised hypohidrotic ectodermal dysplasia
J Jaeken, L Emmery, M Casteels-van Daele
Clinical Dysmorphology
|
May 18, 1999
Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocation
T Lukusa, K Devriendt, J Jaeken, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 14, 1991
Reference values for free gamma-aminobutyric acid determined by ion-exchange chromatography and fluorescence detection in the cerebrospinal fluid of children
H A Carchon, J Jaeken, E Jansen, et al.
Page
of 26