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Results: 1-17 |
Results: 17
Anophthalmia/microphtalmia associated with right lateral facial cleft/microtia
Authors: Fryns, JP Witters, I
Citation: Jp. Fryns et I. Witters, Anophthalmia/microphtalmia associated with right lateral facial cleft/microtia, GEN COUNSEL, 12(2), 2001, pp. 177-178
Cystic hygroma colli as the first echographic sign of the fetal akinesia sequence
Authors: Witters, I Moerman, P Van Assche, FA Fryns, JP
Citation: I. Witters et al., Cystic hygroma colli as the first echographic sign of the fetal akinesia sequence, GEN COUNSEL, 12(1), 2001, pp. 91-94
Sex chromosome Pentasomy (49,XXXXY) presenting with generalized oedema andhypogenitalism at 12 weeks
Authors: Witters, I Moerman, P Braet, P Van Schoubroeck, D Fryns, JP
Citation: I. Witters et al., Sex chromosome Pentasomy (49,XXXXY) presenting with generalized oedema andhypogenitalism at 12 weeks, GEN COUNSEL, 12(1), 2001, pp. 105-106
Prenatal diagnosis of non-obstructive megacystis as part of the megacystis-microcolon-intestinal hypoperistalsis syndrome with favourable postnatal outcome
Authors: Witters, I Theyskens, C van Hoestenberghe, R Sieprath, P Gyselaers, W Fryns, JP
Citation: I. Witters et al., Prenatal diagnosis of non-obstructive megacystis as part of the megacystis-microcolon-intestinal hypoperistalsis syndrome with favourable postnatal outcome, PRENAT DIAG, 21(8), 2001, pp. 704-706
Semilobar holoprosencephaly in a 46,XY female fetus
Authors: Witters, I Moerman, P Muenke, M Van Assche, FA Devriendt, K Legius, E Van Schoubroeck, D Fryns, JP
Citation: I. Witters et al., Semilobar holoprosencephaly in a 46,XY female fetus, PRENAT DIAG, 21(10), 2001, pp. 839-841
Prenatal diagnosis of facial clefting as part of the oculo-auriculo-vertebral spectrum
Authors: Witters, I Schreurs, J Van Wing, J Wouters, W Fryns, JP
Citation: I. Witters et al., Prenatal diagnosis of facial clefting as part of the oculo-auriculo-vertebral spectrum, PRENAT DIAG, 21(1), 2001, pp. 62-64
Bilateral tibial agenesis with ectrodactyly (OMIM 119100): Further evidence for autosomal recessive inheritance
Authors: Witters, I Devriendt, K Moerman, P Caudron, J Van Hole, C Fryns, JP
Citation: I. Witters et al., Bilateral tibial agenesis with ectrodactyly (OMIM 119100): Further evidence for autosomal recessive inheritance, AM J MED G, 104(3), 2001, pp. 209-213
Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic hernia
Authors: Witters, I Legius, E Moerman, P Deprest, J Van Schoubroeck, D Timmerman, D Van Assche, FA Fryns, JP
Citation: I. Witters et al., Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic hernia, AM J MED G, 103(4), 2001, pp. 278-282
Pregnancy outcome and long term prognosis in 868 children born after second trimester amniocentesis for maternal serum positive triple test screeningand normal prenatal karyotype
Authors: Witters, I Legius, E Devriendt, K Moerman, P Van Schoubroeck, D Van Assche, A Fryns, JP
Citation: I. Witters et al., Pregnancy outcome and long term prognosis in 868 children born after second trimester amniocentesis for maternal serum positive triple test screeningand normal prenatal karyotype, J MED GENET, 38(5), 2001, pp. 336-338
Cytomegalovirus reactivation in pregnancy and subsequent isolated bilateral hearing loss in the infant
Authors: Witters, I Van Ranst, M Fryns, JP
Citation: I. Witters et al., Cytomegalovirus reactivation in pregnancy and subsequent isolated bilateral hearing loss in the infant, GEN COUNSEL, 11(4), 2000, pp. 375-378
Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndrome
Authors: Witters, I Moerman, P Fryns, JP
Citation: I. Witters et al., Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndrome, GEN COUNSEL, 11(3), 2000, pp. 215-219
Prenatal diagnosis of central nervous system abnormalities: Diagnostic possibilities and limitations of fetal neurosonography
Authors: Witters, I Fryns, JP
Citation: I. Witters et Jp. Fryns, Prenatal diagnosis of central nervous system abnormalities: Diagnostic possibilities and limitations of fetal neurosonography, GEN COUNSEL, 11(1), 2000, pp. 3-11
Cystic hygroma colli in triplo-X syndrome
Authors: Witters, I Moerman, P Jankelevitch, E Van Assche, A Fryns, JP
Citation: I. Witters et al., Cystic hygroma colli in triplo-X syndrome, GEN COUNSEL, 11(1), 2000, pp. 61-62
Diaphragmatic hernia as the first echographic sign in Apert syndrome
Authors: Witters, I Devriendt, K Moerman, P van Hole, C Fryns, JP
Citation: I. Witters et al., Diaphragmatic hernia as the first echographic sign in Apert syndrome, PRENAT DIAG, 20(5), 2000, pp. 404-406
Laser coagulation of superficial vascular anastomosis in twin-to-twin transfusion syndrome - Authors' reply
Authors: Deprest, J Gratacos, E Witters, I Van Schoubroeck, D Ville, Y Dommergues, M Hecher, K
Citation: J. Deprest et al., Laser coagulation of superficial vascular anastomosis in twin-to-twin transfusion syndrome - Authors' reply, ULTRASOUN O, 13(4), 1999, pp. 285-286
IGF-I, IGF-II, IGF binding protein 1, and C-peptide in second trimester amniotic fluid are dependent on gestational age but do not predict weight at birth
Authors: Verhaeghe, J Coopmans, W Van Herck, E Van Schoubroeck, D Deprest, JA Witters, I
Citation: J. Verhaeghe et al., IGF-I, IGF-II, IGF binding protein 1, and C-peptide in second trimester amniotic fluid are dependent on gestational age but do not predict weight at birth, PEDIAT RES, 46(1), 1999, pp. 101-108
Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiography
Authors: Witters, I Van Buggenhout, G Moerman, P Fryns, JP
Citation: I. Witters et al., Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiography, PRENAT DIAG, 18(12), 1998, pp. 1304-1307
Risultati: 1-17 |