Gewillig M - Search Results

1

Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients.

Rauch A, Devriendt K, Koch A, Rauch R, Gewillig M, Kraus C, Weyand M, Singer H, Reis A, Hofbeck M. Rauch A, et al. Among authors: gewillig m. J Med Genet. 2004 Apr;41(4):e40. doi: 10.1136/jmg.2003.010975. J Med Genet. 2004. PMID: 15060116 Free PMC article. No abstract available.

2

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

3

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.

4

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.

5

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

6

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.

7

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

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: 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

9

Familial deletions of chromosome 22q11: the Leuven experience.

Swillen A, Devriendt K, Vantrappen G, Vogels A, Rommel N, Fryns JP, Eyskens B, Gewillig M, Dumoulin M. Swillen A, et al. Among authors: gewillig m. Am J Med Genet. 1998 Dec 28;80(5):531-2. Am J Med Genet. 1998. PMID: 9880224 No abstract available.

10

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

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