Swillen A - Search Results

1

PTEN mutation in a family with Cowden syndrome and autism.

Goffin A, Hoefsloot LH, Bosgoed E, Swillen A, Fryns JP. Goffin A, et al. Among authors: swillen a. Am J Med Genet. 2001 Aug 8;105(6):521-4. doi: 10.1002/ajmg.1477. Am J Med Genet. 2001. PMID: 11496368

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

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.

8

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

9

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. 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.

10

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

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

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