Ghent University Academic Bibliography

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The Belgian MicroArray Prenatal (BEMAPRE) database : a systematic nationwide repository of fetal genomic aberrations

Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker, et al.

(2018) PRENATAL DIAGNOSIS. 38(13). p.1120-1128
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Outcome after prenatal and postnatal diagnosis of complex congenital heart defects and the influence of genetic anomalies

Katya De Groote (UGent) , Ellen Vanhie (UGent) , Ellen Roets (UGent) , Paul Ramaekers (UGent) , Hans De Wilde (UGent) , Joseph Panzer (UGent) , Kristof Vandekerckhove (UGent) , Thierry Bové (UGent) , Katrien Francois (UGent) , Koen Van Herck (UGent) , et al.

(2017) PRENATAL DIAGNOSIS. 37(10). p.983-991
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Role of CGH array in the diagnosis of autosomal recessive disease : a case of Ellis-van Creveld syndrome

Valentina D'Ambrosio, Carmela Votino, Teresa Cos, Sebastien Boulanger, Annelies Dheedene (UGent) , Jacques Jani and Kathelijn Keymolen

(2015) PRENATAL DIAGNOSIS. 35(1). p.97-99
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First trimester screening for intra-uterine growth restriction and early-onset pre-eclampsia

Griet Vandenberghe (UGent) , I Mensink, JWR Twisk, MA Blankenstein, AC Heijboer and JMG van Vugt

(2011) PRENATAL DIAGNOSIS. 31(10). p.955-961
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- conference
- P1
Current controversies in prenatal diagnosis: does industry sponsorship accelerate or hinder the pace of research?

Sigrid Sterckx (UGent) , Gajus Worthington and André Van Steirteghem

(2011) PRENATAL DIAGNOSIS, 15th Meeting of the Internatioinal-Society-for-Prenatal-Diagnosis-and-Fetal-Therapy, Proceedings paper. 31(3). p.244-245
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- journalArticle
- A1
Prenatal ultrasound and magnetic resonance imaging in fetal varicella syndrome: correlation with pathology findings

Hans Verstraelen (UGent) , B VANZIELEGHEM, Paul Defoort (UGent) , Piet Vanhaesebrouck (UGent) and Marleen Temmerman (UGent)

(2003) PRENATAL DIAGNOSIS. 23(9). p.705-709
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Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS).

Bart Loeys (UGent) , Lieve Nuytinck (UGent) , Petra Van Acker (UGent) , SOPHIE WALRAEDT (UGent) , M BONDUELLE, K SERMON, B HAMEL, A SANCHEZ, Ludwine Messiaen and Anne De Paepe (UGent)

(2002) PRENATAL DIAGNOSIS. 22(1). p.22-28
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- journalArticle
- A1
Personal desires of patients and social obligations of geneticists: applying preimplantation genetic diagnosis for non-medical sex selection

Guido Pennings (UGent)

(2002) PRENATAL DIAGNOSIS. 22(12). p.1123-1129
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- journalArticle
- A1
Prenatal diagnosis of osteogenesis imperfecta type I by COL1A1 null-allele testing.

Lieve Nuytinck (UGent) , BS SAYLI, W. Karen and Anne De Paepe (UGent)

(1999) PRENATAL DIAGNOSIS. 19(9). p.873-875
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- journalArticle
- A1
Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples.

Rudy Van Coster (UGent) , Sandra Janssens (UGent) , JP MISSON, A VERLOES and Juliaan Leroy

(1998) PRENATAL DIAGNOSIS. 18(10). p.1041-1044

Academic Bibliography

The Belgian MicroArray Prenatal (BEMAPRE) database : a systematic nationwide repository of fetal genomic aberrations

Outcome after prenatal and postnatal diagnosis of complex congenital heart defects and the influence of genetic anomalies

Role of CGH array in the diagnosis of autosomal recessive disease : a case of Ellis-van Creveld syndrome

First trimester screening for intra-uterine growth restriction and early-onset pre-eclampsia

Current controversies in prenatal diagnosis: does industry sponsorship accelerate or hinder the pace of research?

Prenatal ultrasound and magnetic resonance imaging in fetal varicella syndrome: correlation with pathology findings

Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS).

Personal desires of patients and social obligations of geneticists: applying preimplantation genetic diagnosis for non-medical sex selection

Prenatal diagnosis of osteogenesis imperfecta type I by COL1A1 null-allele testing.

Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples.

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