Vogels A - Search Results

1

The clinical relevance of intragenic NRXN1 deletions.

Cosemans N, Vandenhove L, Vogels A, Devriendt K, Van Esch H, Van Buggenhout G, Olivié H, de Ravel T, Ortibus E, Legius E, Aerssens P, Breckpot J, R Vermeesch J, Shen S, Fitzgerald J, Gallagher L, Peeters H. Cosemans N, et al. Among authors: vogels a. J Med Genet. 2020 May;57(5):347-355. doi: 10.1136/jmedgenet-2019-106448. Epub 2020 Jan 13. J Med Genet. 2020. PMID: 31932357

2

Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).

Claes S, Vogels A, Holvoet M, Devriendt K, Raeymaekers P, Cassiman JJ, Fryns JP. Claes S, et al. Among authors: vogels a. Am J Med Genet. 1997 Dec 31;73(4):474-9. Am J Med Genet. 1997. PMID: 9415477

3

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: vogels a. Am J Med Genet. 1998 Dec 28;80(5):531-2. Am J Med Genet. 1998. PMID: 9880224 No abstract available.

4

The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescents.

Vogels A, Devriendt K, Legius E, Decock P, Marien J, Hendrickx G, Fryns JP. Vogels A, et al. Genet Couns. 1998;9(4):245-53. Genet Couns. 1998. PMID: 9894160

5

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.

Swillen A, Devriendt K, Legius E, Prinzie P, Vogels A, Ghesquière P, Fryns JP. Swillen A, et al. Among authors: vogels a. Genet Couns. 1999;10(1):79-88. Genet Couns. 1999. PMID: 10191433 Review.

6

Cryptic translocation t(5;18) in familial mental retardation.

Vogels A, Devriendt K, Vermeesch JR, Van Dael R, Marynen P, Dewaele P, Hageman J, Holvoet M, Fryns JP. Vogels A, et al. Ann Genet. 2000 Jul-Dec;43(3-4):117-23. doi: 10.1016/s0003-3995(00)01024-8. Ann Genet. 2000. PMID: 11164192

7

Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications.

Swillen A, Vogels A, Devriendt K, Fryns JP. Swillen A, et al. Among authors: vogels a. Am J Med Genet. 2000 Summer;97(2):128-35. doi: 10.1002/1096-8628(200022)97:2<128::aid-ajmg4>3.0.co;2-z. Am J Med Genet. 2000. PMID: 11180220 Review.

8

The psychopathological phenotype of velo-cardio-facial syndrome.

Vogels A, Verhoeven WM, Tuinier S, DeVriendt K, Swillen A, Curfs LM, Frijns JP. Vogels A, et al. Ann Genet. 2002 Apr-Jun;45(2):89-95. doi: 10.1016/s0003-3995(02)01114-0. Ann Genet. 2002. PMID: 12119217 Review.

9

Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome.

Vogels A, Matthijs G, Legius E, Devriendt K, Fryns JP. Vogels A, et al. J Med Genet. 2003 Jan;40(1):72-3. doi: 10.1136/jmg.40.1.72. J Med Genet. 2003. PMID: 12525547 Free PMC article. No abstract available.

10

Personality profiles of children and adolescents with neurofibromatosis type 1.

Prinzie P, Descheemaeker MJ, Vogels A, Cleymans T, Haselager GJ, Curfs LM, Hellinckx W, Onghena P, Legius E, van Lieshout CF, Fryns JP. Prinzie P, et al. Among authors: vogels a. Am J Med Genet A. 2003 Apr 1;118A(1):1-7. doi: 10.1002/ajmg.a.10003. Am J Med Genet A. 2003. PMID: 12605433

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