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Author/Creator Postma, Alex V.

11. Terminal osseous dysplasia with pigmentary defects and cardiomyopathy caused by a novel FLNA variant. Issue 12 (13th July 2021)

Authors:
Rumping, Lynne; Wessels, Marja W.; Postma, Alex V.; van Schuppen, Joost; van Slegtenhorst, Marjon A.; Saris, Jasper J.; van Tintelen, J. Peter; Robertson, Stephen P.; Alders, Mariëlle; Maas, Saskia M.; Deprez, Ronald H. Lekanne
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 12(2021)
Page Start:
3814
Record Type:
Journal Article
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12. The value of the clinical geneticist caring for adults with congenital heart disease: Diagnostic yield and patients' perspective. Issue 7 (21st May 2013)

Authors:
van Engelen, Klaartje; Baars, Marieke J.H.; Felix, Joyce P.; Postma, Alex V.; Mulder, Barbara J.M.; Smets, Ellen M.A.
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 7(2013:Jul.)
Page Start:
1628
Record Type:
Journal Article
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13. Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy. (3rd November 2016)

Authors:
Jansweijer, Joeri A.; Nieuwhof, Karin; Russo, Francesco; Hoorntje, Edgar T.; Jongbloed, Jan D.H.; Lekanne Deprez, Ronald H.; Postma, Alex V.; Bronk, Marieke; van Rijsingen, Ingrid A.W.; de Haij, Simone; Biagini, Elena; van Haelst, Paul L.; van Wijngaarden, Jan; van den Berg, Maarten P.; Wilde, Ar...
Journal:
European journal of heart failure
Issue:
Volume 19:Number 4(2017)
Page Start:
512
Record Type:
Journal Article
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14. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot. Issue 4 (15th February 2019)

Authors:
Page, Donna J.; Miossec, Matthieu J.; Williams, Simon G.; Monaghan, Richard M.; Fotiou, Elisavet; Cordell, Heather J.; Sutcliffe, Louise; Topf, Ana; Bourgey, Mathieu; Bourque, Guillaume; Eveleigh, Robert; Dunwoodie, Sally L.; Winlaw, David S.; Bhattacharya, Shoumo; Breckpot, Jeroen; Devriendt, Ko...
Journal:
Circulation research
Issue:
Volume 124:Issue 4(2019)
Page Start:
Record Type:
Journal Article
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15. Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy. (October 2018)

Authors:
De Bortoli, Marzia; Postma, Alex V.; Poloni, Giulia; Calore, Martina; Minervini, Giovanni; Mazzotti, Elisa; Rigato, Ilaria; Ebert, Micaela; Lorenzon, Alessandra; Vazza, Giovanni; Cipriani, Alberto; Bariani, Riccardo; Perazzolo Marra, Martina; Husser, Daniela; Thiene, Gaetano; Daliento, Luciano; C...
Journal:
Circulation
Issue:
Volume 11:Number 10(2018)
Page Start:
Record Type:
Journal Article
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