Devriendt K - Search Results

1

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

Muys J, Blaumeiser B, Jacquemyn Y, Bandelier C, Brison N, Bulk S, Chiarappa P, Courtens W, De Leener A, De Rademaeker M, Désir J, Destrée A, Devriendt K, Dheedene A, Fieuw A, Fransen E, Gatot JS, Holmgren P, Jamar M, Janssens S, Keymolen K, Lederer D, Menten B, Meuwissen M, Parmentier B, Pichon B, Rombout S, Sznajer Y, Van Den Bogaert A, Van Den Bogaert K, Vanakker O, Vermeesch J, Janssens K. Muys J, et al. Among authors: devriendt k. Prenat Diagn. 2018 Dec;38(13):1120-1128. doi: 10.1002/pd.5373. Epub 2018 Nov 14. Prenat Diagn. 2018. PMID: 30334587

2

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. 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

3

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.

Devriendt K, Petit P, Matthijs G, Vermeesch JR, Holvoet M, De Muelenaere A, Marynen P, Cassiman JJ, Fryns JP. Devriendt K, et al. J Med Genet. 1997 May;34(5):395-9. doi: 10.1136/jmg.34.5.395. J Med Genet. 1997. PMID: 9152837 Free PMC article.

4

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. 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

5

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. Prenat Diagn. 1998 Jan;18(1):68-72. Prenat Diagn. 1998. PMID: 9483643

6

Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation.

Petit P, Devriendt K, Vermeesch JR, De Cock P, Fryns JP. Petit P, et al. Among authors: devriendt k. Ann Genet. 1998;41(1):22-6. Ann Genet. 1998. PMID: 9599647

7

The prenatal diagnosis of spinal muscular atrophy.

Matthijs G, Devriendt K, Fryns JP. Matthijs G, et al. Among authors: devriendt k. Prenat Diagn. 1998 Jun;18(6):607-10. Prenat Diagn. 1998. PMID: 9664607 Review. No abstract available.

8

The annual incidence of DiGeorge/velocardiofacial syndrome.

Devriendt K, Fryns JP, Mortier G, van Thienen MN, Keymolen K. Devriendt K, et al. J Med Genet. 1998 Sep;35(9):789-90. doi: 10.1136/jmg.35.9.789-a. J Med Genet. 1998. PMID: 9733045 Free PMC article. No abstract available.

9

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).

Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP. Petit P, et al. Among authors: devriendt k. Genet Couns. 1998;9(3):215-21. Genet Couns. 1998. PMID: 9777345

10

Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism.

Devriendt K, Keymolen K, Roelen L, Van Goethem G, Meireleire J, Fryns JP. Devriendt K, et al. Clin Dysmorphol. 2000 Apr;9(2):111-4. doi: 10.1097/00019605-200009020-00007. Clin Dysmorphol. 2000. PMID: 10826622

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