Fryns JP - Search Results

1

Cerebellar hypoplasia in a patient with velo-cardio-facial syndrome.

Devriendt K, Thienen MN, Swillen A, Fryns JP. Devriendt K, et al. Among authors: fryns jp. Dev Med Child Neurol. 1996 Oct;38(10):949-53. doi: 10.1111/j.1469-8749.1996.tb15052.x. Dev Med Child Neurol. 1996. PMID: 8870617

2

Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defect.

Swillen A, Feys H, Adriaens T, Nelissen L, Mertens L, Gewillig M, Devriendt K, Fryns JP. Swillen A, et al. Among authors: fryns jp. Dev Med Child Neurol. 2005 Dec;47(12):797-802. doi: 10.1017/S0012162205001696. Dev Med Child Neurol. 2005. PMID: 16288668 Free article.

3

Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome).

Van Aken K, De Smedt B, Van Roie A, Gewillig M, Devriendt K, Fryns JP, Simons J, Swillen A. Van Aken K, et al. Among authors: fryns jp. Dev Med Child Neurol. 2007 Mar;49(3):210-3. doi: 10.1111/j.1469-8749.2007.00210.x. Dev Med Child Neurol. 2007. PMID: 17355478 Free article.

4

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: fryns jp. Ann Genet. 1995;38(4):228-30. Ann Genet. 1995. PMID: 8629811

5

Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndrome.

Devriendt K, D'Espallier L, Fryns JP. Devriendt K, et al. Among authors: fryns jp. J Med Genet. 1996 Mar;33(3):224-6. doi: 10.1136/jmg.33.3.224. J Med Genet. 1996. PMID: 8728696 Free PMC article.

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: fryns jp. 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

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

8

Deletion in chromosome region 22q11 in a child with CHARGE association.

Devriendt K, Swillen A, Fryns JP. Devriendt K, et al. Among authors: fryns jp. Clin Genet. 1998 May;53(5):408-10. doi: 10.1111/j.1399-0004.1998.tb02755.x. Clin Genet. 1998. PMID: 9660062

9

Further delineation of the KBG syndrome.

Devriendt K, Holvoet M, Fryns JP. Devriendt K, et al. Among authors: fryns jp. Genet Couns. 1998;9(3):191-4. Genet Couns. 1998. PMID: 9777340

10

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: fryns jp. Genet Couns. 1999;10(1):3-9. Genet Couns. 1999. PMID: 10191424 Review.

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