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Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|October 6, 2016
The effect of losartan therapy on ventricular function in Marfan patients with haploinsufficient or dominant negative FBN1 mutationsA W den Hartog, R Franken, M P van den Berg, et al.
The Journal of Pathology|December 18, 2001
Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancerJ M Piek, P J van Diest, R P Zweemer, et al.
Prenatal Diagnosis|April 1, 1996
Early prenatal diagnosis of Fanconi anaemia in a twin pregnancy, using DNA analysisM L Kwee, J R Lo Ten Foe, F Arwert, et al.
Clinical Genetics|July 19, 2012
An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three-generation family at serious risk for aortic dissectionY Hilhorst-Hofstee, A J H A Scholte, M E B Rijlaarsdam, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
Anticipation in familial intracranial aneurysms in consecutive generationsP M Struycken, G Pals, M Limburg, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|March 5, 2010
Recurrent and founder mutations in the Netherlands: Extensive clinical variability in Marfan syndrome patients with a single novel recurrent fibrillin-1 missense mutationJ J J Aalberts, A G Schuurman, G Pals, et al.
Hypertension in Pregnancy|June 5, 2002
Linkage and association studies of IL1B and IL1RN gene polymorphisms in preeclampsiaAugusta M A Lachmeijer, Maria P Nosti-Escanilla, Esther B Bastiaans, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
A genome-wide scan for preeclampsia in the NetherlandsA M Lachmeijer, R Arngrímsson, E J Bastiaans, et al.
Stroke|August 28, 2004
Genome-wide linkage in a large Dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13Y B W E M Roos, G Pals, P M Struycken, et al.
British Journal of Cancer|October 10, 2002
Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approachJ J P Gille, F B L Hogervorst, G Pals, et al.
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