Gewillig M - Search Results

1

Rare variants in NR2F2 cause congenital heart defects in humans.

Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LC, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Low J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, Fitzpatrick DF; UK10K Consortium; Wilson DI, Mital S, Hurles ME. Al Turki S, et al. Among authors: gewillig m. Am J Hum Genet. 2014 Apr 3;94(4):574-85. doi: 10.1016/j.ajhg.2014.03.007. Am J Hum Genet. 2014. PMID: 24702954 Free PMC article.

2

Asplenia syndrome and isolated total anomalous pulmonary venous connection in siblings.

Devriendt K, Casaer A, Van Cauter A, de Zegher F, Dumoulin M, Gewillig M, Devlieger H. Devriendt K, et al. Among authors: gewillig m. Eur J Pediatr. 1994 Oct;153(10):712-4. doi: 10.1007/BF01954484. Eur J Pediatr. 1994. PMID: 7813525

3

Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome.

Devriendt K, De Mars K, De Cock P, Gewillig M, Fryns JP. Devriendt K, et al. Among authors: gewillig m. Ann Genet. 1995;38(4):228-30. Ann Genet. 1995. PMID: 8629811

4

Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletion.

Devriendt K, Van Hoestenberghe R, Van Hole C, Devlieger H, Gewillig M, Moerman P, Van den Berghe H, Fryns JP. Devriendt K, et al. Among authors: gewillig m. Clin Genet. 1997 Apr;51(4):246-9. doi: 10.1111/j.1399-0004.1997.tb02463.x. Clin Genet. 1997. PMID: 9184246

5

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

Swillen A, Devriendt K, Legius E, Eyskens B, Dumoulin M, Gewillig M, Fryns JP. Swillen A, et al. Among authors: gewillig m. J Med Genet. 1997 Jun;34(6):453-8. doi: 10.1136/jmg.34.6.453. J Med Genet. 1997. PMID: 9192263 Free PMC article.

6

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8.

Claeys I, Holvoet M, Eyskens B, Adriaensens P, Gewillig M, Fryns JP, Devriendt K. Claeys I, et al. Among authors: gewillig m. Am J Med Genet. 1997 Sep 19;74(5):515-20. doi: 10.1002/(sici)1096-8628(19970919)74:5<515::aid-ajmg12>3.0.co;2-f. Am J Med Genet. 1997. PMID: 9342203

7

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: gewillig m. 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

8

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

9

Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes.

Petit P, Devriendt K, Azou M, Gewillig M, Fryns JP. Petit P, et al. Among authors: gewillig m. Genet Couns. 1998;9(4):271-5. Genet Couns. 1998. PMID: 9894164

10

Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.

Devriendt K, Matthijs G, Van Dael R, Gewillig M, Eyskens B, Hjalgrim H, Dolmer B, McGaughran J, Bröndum-Nielsen K, Marynen P, Fryns JP, Vermeesch JR. Devriendt K, et al. Among authors: gewillig m. Am J Hum Genet. 1999 Apr;64(4):1119-26. doi: 10.1086/302330. Am J Hum Genet. 1999. PMID: 10090897 Free PMC article.

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