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Comparative Biochemistry and Physiology. B, Comparative Biochemistry
|
January 1, 1988
Comparative studies on the low density lipoprotein subfractions from pig and man
D W Swinkels, P N Demacker
Nederlands Tijdschrift Voor Geneeskunde
|
July 28, 1999
[Diagnosis and treatment of primary hemochromatosis]
D W Swinkels, J J Marx
Nederlands Tijdschrift Voor Geneeskunde
|
April 26, 2003
[From gene to disease; HFE-mutations in primary haemochromatosis]
D W Swinkels, E M G Jacobs
Best Practice & Research. Clinical Gastroenterology
|
May 6, 2009
Hereditary haemochromatosis
M C H Janssen, D W Swinkels
Nederlands Tijdschrift Voor Geneeskunde
|
March 9, 1996
[Fecal analysis for occult blood obsolete]
D W Swinkels, H Wollersheim, J L Willems
Nederlands Tijdschrift Voor Geneeskunde
|
December 6, 2003
[The prioritization of genetic screening with primary haemochromatosis as an example]
E M Jacobs, A L Verbeek, D W Swinkels
Prenatal Diagnosis
|
July 18, 2003
Increased total cell-free DNA in the serum of pregnant women carrying a fetus affected by trisomy 21
Kevin Spencer, J B de Kok, D W Swinkels
Nederlands Tijdschrift Voor Geneeskunde
|
July 12, 1997
[Hereditary haemochromatosis: recent developments in diagnostics]
D W Swinkels, M P Cooreman, W W van Solinge
Anticancer Research
|
August 23, 2000
Clinical value of bile for the detection of mutant K-ras from colorectal liver metastases
J B de Kok, D W Swinkels, T J Ruers
Acta Haematologica
|
January 1, 1997
The characterisation of leukaemias with the Sysmex NE-8000
W van der Meer, D W Swinkels, H L Willems
Page
of 8
Search research articles
Search
Showing results (1-10 of 74) with videos related to
Sort By:
Page
of 8
Comparative Biochemistry and Physiology. B, Comparative Biochemistry
|
January 1, 1988
Comparative studies on the low density lipoprotein subfractions from pig and man
D W Swinkels, P N Demacker
Nederlands Tijdschrift Voor Geneeskunde
|
July 28, 1999
[Diagnosis and treatment of primary hemochromatosis]
D W Swinkels, J J Marx
Nederlands Tijdschrift Voor Geneeskunde
|
April 26, 2003
[From gene to disease; HFE-mutations in primary haemochromatosis]
D W Swinkels, E M G Jacobs
Best Practice & Research. Clinical Gastroenterology
|
May 6, 2009
Hereditary haemochromatosis
M C H Janssen, D W Swinkels
Nederlands Tijdschrift Voor Geneeskunde
|
March 9, 1996
[Fecal analysis for occult blood obsolete]
D W Swinkels, H Wollersheim, J L Willems
Nederlands Tijdschrift Voor Geneeskunde
|
December 6, 2003
[The prioritization of genetic screening with primary haemochromatosis as an example]
E M Jacobs, A L Verbeek, D W Swinkels
Prenatal Diagnosis
|
July 18, 2003
Increased total cell-free DNA in the serum of pregnant women carrying a fetus affected by trisomy 21
Kevin Spencer, J B de Kok, D W Swinkels
Nederlands Tijdschrift Voor Geneeskunde
|
July 12, 1997
[Hereditary haemochromatosis: recent developments in diagnostics]
D W Swinkels, M P Cooreman, W W van Solinge
Anticancer Research
|
August 23, 2000
Clinical value of bile for the detection of mutant K-ras from colorectal liver metastases
J B de Kok, D W Swinkels, T J Ruers
Acta Haematologica
|
January 1, 1997
The characterisation of leukaemias with the Sysmex NE-8000
W van der Meer, D W Swinkels, H L Willems
Page
of 8