Gewillig M - Search Results

1

Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.

Vantrappen G, Devriendt K, Swillen A, Rommel N, Vogels A, Eyskens B, Gewillig M, Feenstra L, Fryns JP. Vantrappen G, et al. Among authors: gewillig m. Genet Couns. 1999;10(1):3-9. Genet Couns. 1999. PMID: 10191424 Review.

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

Renal and urological tract malformations caused by a 22q11 deletion.

Devriendt K, Swillen A, Fryns JP, Proesmans W, Gewillig M. Devriendt K, et al. Among authors: gewillig m. J Med Genet. 1996 Apr;33(4):349. doi: 10.1136/jmg.33.4.349. J Med Genet. 1996. PMID: 8730297 Free PMC article. No abstract available.

5

The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease.

Devriendt K, Eyskens B, Swillen A, Dumoulin M, Gewillig M, Fryns JP. Devriendt K, et al. Among authors: gewillig m. Eur J Pediatr. 1996 Aug;155(8):721. doi: 10.1007/BF01957162. Eur J Pediatr. 1996. PMID: 8839734 No abstract available.

6

Polyhydramnios and paroxysmal atrial tachycardia as first clinical signs in Costello syndrome.

Fryns JP, Devlieger H, Gewillig M, Lukusa P, Devriendt K. Fryns JP, et al. Among authors: gewillig m. Genet Couns. 1996;7(3):237-9. Genet Couns. 1996. PMID: 8897048 No abstract available.

7

Cardiac strangulation, a rare complication of epicardial pacemaker leads during growth.

Eyskens B, Mertens L, Moerman P, Ector H, Daenen W, Gewillig M. Eyskens B, et al. Among authors: gewillig m. Heart. 1997 Mar;77(3):288-9. doi: 10.1136/hrt.77.3.288. Heart. 1997. PMID: 9093054 Free PMC article.

8

Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?

Devriendt K, Naulaers G, Matthijs G, Van Houdt K, Devlieger H, Gewillig M, Fryns JP. Devriendt K, et al. Among authors: gewillig m. Ann Genet. 1997;40(1):14-7. Ann Genet. 1997. PMID: 9150845

9

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

10

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.

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