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Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
January 1, 1995
Radiation tolerance of normal mouse bladders after intravesical chemotherapy
J G Post, J A te Poele, Y G Oussoren, et al.
Bioinformatics (Oxford, England)
|
September 21, 2007
A semantic web approach applied to integrative bioinformatics experimentation: a biological use case with genomics data
Lennart J G Post, Marco Roos, M Scott Marshall, et al.
Journal of Hepatology
|
February 1, 1988
Bone disease after orthotopic liver transplantation
E B Haagsma, C J Thijn, J G Post, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
September 3, 2021
Family screening in patients with isolated bicuspid aortic valve : Restriction to those with aortic dilatation is not justified
L Cozijnsen, R L Braam, M Bakker-de Boo, et al.
American Journal of Medical Genetics
|
June 5, 1995
Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis)
P E Taschner, N de Vos, J G Post, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
October 2, 2008
The many faces of aggressive aortic pathology: Loeys-Dietz syndrome
J J J Aalberts, M P van den Berg, J E H Bergman, et al.
Journal of Medical Genetics
|
February 1, 1993
The fragile X syndrome: no evidence for any recent mutations
A P Smits, J C Dreesen, J G Post, et al.
Gastroenterology
|
May 29, 2001
Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms
Y Wu, M J Berends, J G Post, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
April 10, 2013
Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy
P A van der Zwaag, I A W van Rijsingen, R de Ruiter, et al.
Clinical Genetics
|
July 13, 2010
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
D L Smit, A R Mensenkamp, S Badeloe, et al.
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 20 results.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
January 1, 1995
Radiation tolerance of normal mouse bladders after intravesical chemotherapy
J G Post, J A te Poele, Y G Oussoren, et al.
Bioinformatics (Oxford, England)
|
September 21, 2007
A semantic web approach applied to integrative bioinformatics experimentation: a biological use case with genomics data
Lennart J G Post, Marco Roos, M Scott Marshall, et al.
Journal of Hepatology
|
February 1, 1988
Bone disease after orthotopic liver transplantation
E B Haagsma, C J Thijn, J G Post, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
September 3, 2021
Family screening in patients with isolated bicuspid aortic valve : Restriction to those with aortic dilatation is not justified
L Cozijnsen, R L Braam, M Bakker-de Boo, et al.
American Journal of Medical Genetics
|
June 5, 1995
Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis)
P E Taschner, N de Vos, J G Post, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
October 2, 2008
The many faces of aggressive aortic pathology: Loeys-Dietz syndrome
J J J Aalberts, M P van den Berg, J E H Bergman, et al.
Journal of Medical Genetics
|
February 1, 1993
The fragile X syndrome: no evidence for any recent mutations
A P Smits, J C Dreesen, J G Post, et al.
Gastroenterology
|
May 29, 2001
Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms
Y Wu, M J Berends, J G Post, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
April 10, 2013
Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy
P A van der Zwaag, I A W van Rijsingen, R de Ruiter, et al.
Clinical Genetics
|
July 13, 2010
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
D L Smit, A R Mensenkamp, S Badeloe, et al.
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of 2