1.
Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans
by Thienpont, Bernard
American journal of human genetics, 2010, Vol.86 (6), p.839-849
2.
22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia
by van Engelen, Klaartje
Heart, 2010, Vol.96 (8), p.621-624
3.
Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations
by Elfferich, Peter
Neurogenetics, 2011, Vol.12 (4), p.263-271
4.
Bicuspid Aortic Valve Morphology and Associated Cardiovascular Abnormalities in Fetal Turner Syndrome: A Pathomorphological Study
by van Engelen, Klaartje
Fetal diagnosis and therapy, 2014, Vol.36 (1), p.59-68
5.
Prevalence of congenital heart defects in neuroblastoma patients: a cohort study and systematic review of literature
by van Engelen, Klaartje
European journal of pediatrics, 2009, Vol.168 (9), p.1081-1090
6.
The Authors' reply
by van Engelen, Klaartje
Heart (British Cardiac Society), 2011, Vol.97 (10), p.860
7.
The Authors' reply
by van Engelen, Klaartje
Heart (British Cardiac Society), 2011, Vol.97 (10), p.860
8.
The Authors' reply
by Klaartje van Engelen
Heart (British Cardiac Society), 2011, Vol.97 (10), p.860
9.
Bicuspid aortic valve morphology and associated cardiovascular abnormalities in fetal turner syndrome: A pathomorphological study
by Van Engelen, Klaartje
Fetal diagnosis and therapy, 2014, Vol.36 (1), p.59-68
10.
Screening for 22q11.2 microdeletion in adults with tetralogy of Fallot
by Digilio, M Cristina
Heart (British Cardiac Society), 2011, Vol.97 (10), p.860-860
11.
Screening for 22q11.2 microdeletion in adults with tetralogy of Fallot Reply
by van Engelen, Klaartje
Heart (British Cardiac Society), 2011, Vol.97 (10), p.860
12.
Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans
by Thienpont, Bernard
American journal of human genetics, 2010, Vol.86 (6), p.839-849
13.
22q11.2 Deletion syndrome is under-recognised in adult patients with tetralogy of fallot and pulmonary atresia
by Van Engelen, Klaartje
Heart (British Cardiac Society), 2010, Vol.96 (8), p.621-624
14.
Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations
by Elfferich, Peter
Neurogenetics, 2011, Vol.12 (4), p.263-271
15.
Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations
by Elfferich, Peter
Neurogenetics, 2011, Vol.12 (4), p.263-271
16.
Prevalence of congenital heart defects in neuroblastoma patients: a cohort study and systematic review of literature
by van Engelen, Klaartje
European journal of pediatrics, 2009, Vol.168 (9), p.1081-1090
17.
Prevalence of congenital heart defects in neuroblastoma patients: A cohort study and systematic review of literature
by Van Engelen, Klaartje
European journal of pediatrics, 2009, Vol.168 (9), p.1081-1090
