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Health-related quality of life in children and young adults with Marfan syndrome
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Arterial tortuosity syndrome : 40 new families and literature review
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- Journal Article
- A1
- open access
Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia
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Joubert syndrome in three siblings
(2015) TIJDSCHRIFT VAN DE BELGISCHE KINDERARTS. In Tijdschrift van de Belgische kinderarts 17(1). p.93-93 -
- Conference Paper
- C3
- open access
Joubert syndrome in three siblings
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Marfan syndrome
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Randomized trial of atenolol versus losartan in children and young adults with Marfan syndrome
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- Journal Article
- A1
- open access
Atenolol versus losartan in children and young adults with Marfan's syndrome
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Bladder exstrophy-epispadias complex and triple-X syndrome: incidental finding or causality?
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- Journal Article
- A1
- open access
Absence of cardiovascular manifestations in a haploinsufficient TGFBR1 mouse model