Swillen A - 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: swillen a. 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

Fragile X boys: evolution of the mental age in childhood. Preliminary data on 10 prepubertal boys.

Borghgraef M, Swillen A, Van den Berghe H, Fryns JP. Borghgraef M, et al. Among authors: swillen a. Genet Couns. 1995;6(2):97-101. Genet Couns. 1995. PMID: 7546457

3

The Prader-Willi syndrome: a self supporting program for children, youngsters and adults.

Descheemaeker MJ, Swillen A, Plissart L, Borghgraef M, Rasenberg S, Curfs LM, Fryns JP. Descheemaeker MJ, et al. Among authors: swillen a. Genet Couns. 1994;5(2):199-205. Genet Couns. 1994. PMID: 7917134

4

Turner syndrome patients as adults: a study of their cognitive profile, psychosocial functioning and psychopathological findings.

Delooz J, Van den Berghe H, Swillen A, Kleczkowska A, Fryns JP. Delooz J, et al. Among authors: swillen a. Genet Couns. 1993;4(3):169-79. Genet Couns. 1993. PMID: 8267923

5

Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years).

Swillen A, Fryns JP, Kleczkowska A, Massa G, Vanderschueren-Lodeweyckx M, Van den Berghe H. Swillen A, et al. Genet Couns. 1993;4(1):7-18. Genet Couns. 1993. PMID: 8471226

6

The Coffin-Siris syndrome: data on mental development, language, behavior and social skills in 12 children.

Swillen A, Glorieux N, Peeters M, Fryns JP. Swillen A, et al. Clin Genet. 1995 Oct;48(4):177-82. doi: 10.1111/j.1399-0004.1995.tb04084.x. Clin Genet. 1995. PMID: 8591667

7

Neurodevelopmental changes with age in Ullrich-Turner syndrome.

Swillen A, Fryns JP. Swillen A, et al. Am J Med Genet. 1996 Jan 11;61(2):198. doi: 10.1002/ajmg.1320610207. Am J Med Genet. 1996. PMID: 8669456 No abstract available.

8

Autism and genetics: high incidence of specific genetic syndromes in 21 autistic adolescents and adults living in two residential homes in Belgium.

Swillen A, Hellemans H, Steyaert J, Fryns JP. Swillen A, et al. Am J Med Genet. 1996 May 31;67(3):315-6. doi: 10.1002/(SICI)1096-8628(19960531)67:3<315::AID-AJMG9>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8725750 No abstract available.

9

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: swillen a. 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.

10

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: swillen a. Eur J Pediatr. 1996 Aug;155(8):721. doi: 10.1007/BF01957162. Eur J Pediatr. 1996. PMID: 8839734 No abstract available.

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