Fryns JP - Search Results

1

Prenatal diagnosis and pulmonary pathology in congenital high airway obstruction sequence.

Witters I, Fryns JP, De Catte L, Moerman P. Witters I, et al. Among authors: fryns jp. Prenat Diagn. 2009 Nov;29(11):1081-4. doi: 10.1002/pd.2349. Prenat Diagn. 2009. PMID: 19757402 No abstract available.

2

Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).

Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns JP. Witters I, et al. Among authors: fryns jp. Prenat Diagn. 2002 Jan;22(1):29-33. doi: 10.1002/pd.225. Prenat Diagn. 2002. PMID: 11810646

3

Positive maternal serum triple test screening in severe early onset hypophosphatasia.

Witters I, Moerman P, Mornet E, Fryns JP. Witters I, et al. Among authors: fryns jp. Prenat Diagn. 2004 Jul;24(7):494-7. doi: 10.1002/pd.859. Prenat Diagn. 2004. PMID: 15300736

4

Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiopathy.

Witters I, Van Buggenhout G, Moerman P, Fryns JP. Witters I, et al. Among authors: fryns jp. Prenat Diagn. 1998 Dec;18(12):1304-7. Prenat Diagn. 1998. PMID: 9885024

5

Prenatal diagnosis of facial clefting as part of the oculo-auriculo-vertebral spectrum.

Witters I, Schreurs J, Van Wing J, Wouters W, Fryns JP. Witters I, et al. Among authors: fryns jp. Prenat Diagn. 2001 Jan;21(1):62-4. doi: 10.1002/1097-0223(200101)21:1<62::aid-pd969>3.0.co;2-y. Prenat Diagn. 2001. PMID: 11180244

6

Semilobar holoprosencephaly in a 46,XY female fetus.

Witters I, Moerman P, Muenke M, Van Assche FA, Devriendt K, Legius E, Van Schoubroeck D, Fryns JP. Witters I, et al. Among authors: fryns jp. Prenat Diagn. 2001 Oct;21(10):839-41. doi: 10.1002/pd.151. Prenat Diagn. 2001. PMID: 11746125

7

The cardiofaciocutaneous syndrome: prenatal findings in two patients.

Witters I, Denayer E, Brems H, Fryns JP, Legius E. Witters I, et al. Among authors: fryns jp. Prenat Diagn. 2008 Jan;28(1):53-5. doi: 10.1002/pd.1891. Prenat Diagn. 2008. PMID: 18022830 No abstract available.

8

Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndrome.

Witters I, Moerman P, Fryns JP. Witters I, et al. Among authors: fryns jp. Genet Couns. 2000;11(3):215-9. Genet Couns. 2000. PMID: 11043429

9

Post-zygotic origin of isochromosome 12p.

de Ravel TJ, Keymolen K, van Assche E, Wittevronghel I, Moerman P, Salden I, Matthijs G, Fryns JP, Vermeesch JR. de Ravel TJ, et al. Among authors: fryns jp. Prenat Diagn. 2004 Dec 15;24(12):984-8. doi: 10.1002/pd.956. Prenat Diagn. 2004. PMID: 15614858

10

First trimester prenatal diagnosis of 13q-syndrome presenting with increased nuchal translucency, Dandy-Walker malformation and small parietal encephalocoele.

Hindryckx A, De Catte L, Van Esch H, Fryns JP, Moerman P, Devlieger R. Hindryckx A, et al. Among authors: fryns jp. Prenat Diagn. 2008 May;28(5):445-6. doi: 10.1002/pd.1989. Prenat Diagn. 2008. PMID: 18395870 No abstract available.

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