Fryns JP - Search Results

1

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

2

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.

3

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

4

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

5

Lobar holoprosencephaly and Xq22 deletion.

Petit P, Moerman P, Fryns JP. Petit P, et al. Among authors: fryns jp. Genet Couns. 1991;2(2):119-21. Genet Couns. 1991. PMID: 1781956

6

Elevated maternal serum and amniotic fluid alpha-fetoprotein levels in the Denys-Drash syndrome.

Devriendt K, van den Berghe K, Moerman P, Fryns JP. Devriendt K, et al. Among authors: fryns jp. Prenat Diagn. 1996 May;16(5):455-7. doi: 10.1002/(SICI)1097-0223(199605)16:5<455::AID-PD865>3.0.CO;2-S. Prenat Diagn. 1996. PMID: 8844005

7

Diagnostic echographic findings in cryptophthalmos syndrome (Fraser syndrome).

Fryns JP, van Schoubroeck D, Vandenberghe K, Nagels H, Klerckx P. Fryns JP, et al. Prenat Diagn. 1997 Jun;17(6):582-4. doi: 10.1002/(sici)1097-0223(199706)17:6<582::aid-pd107>3.0.co;2-y. Prenat Diagn. 1997. PMID: 9203218

8

Prenatal diagnosis of a terminal short arm deletion of chromosome 8 in a fetus with an atrioventricular septal defect.

Devriendt K, Van Schoubroeck D, Eyskens B, Gewillig M, Vandenberghe K, Fryns JP. Devriendt K, et al. Among authors: fryns jp. Prenat Diagn. 1998 Jan;18(1):65-7. doi: 10.1002/(sici)1097-0223(199801)18:1<65::aid-pd207>3.0.co;2-4. Prenat Diagn. 1998. PMID: 9483642

9

Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndrome.

Devriendt K, Van Schoubroeck D, Eyskens B, Vantrappen G, Swillen A, Gewillig M, Dumoulin M, Moerman P, Vandenberghe K, Fryns JP. Devriendt K, et al. Among authors: fryns jp. Prenat Diagn. 1998 Jan;18(1):68-72. Prenat Diagn. 1998. PMID: 9483643

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,311 results

Search Page

Filters