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Annick Vogels

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Ellen Denayer; Annabel Parret; Magdalena Chmara; Suzanne Schubbert; Annick Vogels; koenraad devriendt; JP Frijns; Vladimir Rybin; T J L de Ravel; Kevin Shannon; Jan Cools; Klaus Scheffzek; Eric Legius
Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation.
Bert De Smedt; koenraad devriendt; Jean-Pierre Fryns; Annick Vogels; Marc Gewillig; Ann Swillen
Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update.
Annick Vogels; Jean-Pierre Fryns
Pfeiffer syndrome.

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2008: Ellen Denayer; Annabel Parret; Magdalena Chmara; Suzanne Schubbert; Annick Vogels; koenraad devriendt; JP Frijns; Vladimir Rybin; T J L de Ravel; Kevin Shannon; Jan Cools; Klaus Scheffzek; Eric Legius
Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation.
Human mutation 2008;29(2):232-9.
2007: Bert De Smedt; koenraad devriendt; Jean-Pierre Fryns; Annick Vogels; Marc Gewillig; Ann Swillen
Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update.
Journal of intellectual disability research : JIDR 2007;51(Pt 9):666-70.
2006: Annick Vogels; Jean-Pierre Fryns
Pfeiffer syndrome.
Orphanet journal of rare diseases 2006;1():19.
2005: Griet Van Buggenhout; Conny van Ravenswaaij-Arts; N Mc Maas; Reinhilde Thoelen; Annick Vogels; Dominique Smeets; Ivo Salden; Gert Matthijs; Jean-Pierre Fryns; Joris R Vermeesch
The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients.
European journal of medical genetics 2005;48(3):276-89.
2005: T Lukusa; Eric E J Smeets; Annick Vogels; Joris R Vermeesch; Jean-Pierre Fryns
Terminal 2q37 deletion and autistic behaviour.
Genetic counseling (Geneva, Switzerland) 2005;16(2):179-80.
2004: Annick Vogels; Marc De Hert; Mie-Jef Descheemaeker; Veerle Govers; koenraad devriendt; Eric Legius; P Prinzie; Jean-Pierre Fryns
Psychotic disorders in Prader-Willi syndrome.
American journal of medical genetics. Part A 2004;127A(3):238-43.
2004: Annick Vogels; Jenneke Van Den Ende; Kathelijn Keymolen; Geert Mortier; koenraad devriendt; Eric Legius; Jean-Pierre Fryns
Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.
European journal of human genetics : EJHG 2004;12(3):238-40.
2004: Annick Vogels; Jean-Pierre Fryns
Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndrome.
Genetic counseling (Geneva, Switzerland) 2004;15(4):397-404.
2004: P Prinzie; Ann Swillen; B Maes; Patrick Onghena; Annick Vogels; A Van Hooste; koenraad devriendt; Cornelis F M Van Lieshout; Jean-Pierre Fryns
Parenting, family contexts, and personality characteristics in youngsters with VCFS.
Genetic counseling (Geneva, Switzerland) 2004;15(2):141-57.
2003: P Prinzie; Mie-Jef Descheemaeker; Annick Vogels; T Cleymans; Gerbert J T Haselager; Leopold M G Curfs; Walter Hellinckx; Patrick Onghena; Eric Legius; Cornelis F M Van Lieshout; Jean-Pierre Fryns
Personality profiles of children and adolescents with neurofibromatosis type 1.
American journal of medical genetics. Part A 2003;118A(1):1-7.
2002: Annick Vogels; W M A Verhoeven; Siegfried Tuinier; koenraad devriendt; Ann Swillen; Leopold M G Curfs; JP Frijns
The psychopathological phenotype of velo-cardio-facial syndrome.
Annales de génétique 2002;45(2):89-95.
2002: Annick Vogels; Jean-Pierre Fryns
The Prader-Willi syndrome and the Angelman syndrome.
Genetic counseling (Geneva, Switzerland) 2002;13(4):385-96.
2002: P Prinzie; Ann Swillen; Annick Vogels; V Kockuyt; Leopold M G Curfs; Gerbert J T Haselager; Walter Hellinckx; koenraad devriendt; Patrick Onghena; Cornelis F M Van Lieshout; Jean-Pierre Fryns
Personality profiles of youngsters with velo-cardio-facial syndrome.
Genetic counseling (Geneva, Switzerland) 2002;13(3):265-80.
2002: Annick Vogels; Jean-Pierre Fryns
The velocardiofacial syndrome: a review.
Genetic counseling (Geneva, Switzerland) 2002;13(2):105-13.
2002: Annick Vogels; Maureen Holvoet; Mie-Jef Descheemaeker; Jean-Pierre Fryns; koenraad devriendt
Atypical presentation of the Prader-Willi syndrome. Mosaic trisomy 15?
Annales de génétique 2002;45(1):1-3.
2002: Mie-Jef Descheemaeker; Annick Vogels; Veerle Govers; Martine Borghgraef; Diane Willekens; Ann Swillen; W M A Verhoeven; Jean-Pierre Fryns
Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrum.
Journal of intellectual disability research : JIDR 2002;46(Pt 1):41-50.
2000: Annick Vogels; koenraad devriendt; Joris R Vermeesch; R Van Dael; Peter Marynen; P Dewaele; J Hageman; Maureen Holvoet; Jean-Pierre Fryns
Cryptic translocation t(5;18) in familial mental retardation.
Annales de génétique 2000;43(3-4):117-23.
2000: Ann Swillen; Annick Vogels; koenraad devriendt; J P Fryns
Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications.
American journal of medical genetics 2000;97(2):128-35.
1999: Ann Swillen; koenraad devriendt; Eric Legius; P Prinzie; Annick Vogels; Pol Ghesquière; Jean-Pierre Fryns
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.
Genetic counseling (Geneva, Switzerland) 1999;10(1):79-88.
1999: Greet Vantrappen; koenraad devriendt; Ann Swillen; Nathalie Rommel; Annick Vogels; Benedicte Eyskens; Marc Gewillig; Louw Feenstra; Jean-Pierre Fryns
Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
Genetic counseling (Geneva, Switzerland) 1999;10(1):3-9.
1998: Ann Swillen; koenraad devriendt; Greet Vantrappen; Annick Vogels; Nathalie Rommel; Jean-Pierre Fryns; Benedicte Eyskens; Marc Gewillig; M Dumoulin
Familial deletions of chromosome 22q11: the Leuven experience.
American journal of medical genetics 1998;80(5):531-2.
1998: David Clarke; Harm Boer; Tessa Webb; P Scott; S Frazer; Annick Vogels; Martine Borghgraef; Leopold M G Curfs
Prader-Willi syndrome and psychotic symptoms: 1. Case descriptions and genetic studies.
Journal of intellectual disability research : JIDR 1998;42 ( Pt 6)():440-50.
1998: Annick Vogels; koenraad devriendt; Eric Legius; P Decock; J Marien; G Hendrickx; J P Fryns
The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescents.
Genetic counseling (Geneva, Switzerland) 1998;9(4):245-53.
1997: Stephan J Claes; Annick Vogels; Maureen Holvoet; koenraad devriendt; Petra Raeymaekers; Jean-Jacques Cassiman; Jean-Pierre Fryns
Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).
American journal of medical genetics 1997;73(4):474-9.
1997: Annick Vogels; J Haegeman; Jean-Pierre Fryns
Pierre-Robin sequence and severe mental retardation with chaotic behaviour associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333)).
Genetic counseling (Geneva, Switzerland) 1997;8(3):249-52.
1996: Annick Vogels; M E Lorenzetti; P Gillis; J P Fryns
Facial asymmetry, cardio-vascular anomalies and adducted thumbs as unusual symptoms in Dubowitz syndrome?
Annales de génétique 1996;39(1):31-4.
1995: D Soekarman; J M Cobben; Annick Vogels; Paul H M Spauwen; J P Fryns
Variable expression of the popliteal pterygium syndrome in two 3-generation families.
Clinical genetics 1995;47(4):169-74.
1994: Annick Vogels; Luc De Smet; Herman Van Den Berghe; J P Fryns
Thrombocytopenia and cleft hand in monosomy 21.
Genetic counseling (Geneva, Switzerland) 1994;5(1):67-71.
1994: J P Fryns; Annick Vogels; J Haegeman; E Eggermont; Herman Van Den Berghe
Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype.
Genetic counseling (Geneva, Switzerland) 1994;5(4):337-43.
1993: J P Fryns; Annick Vogels; P Decock; Herman Van Den Berghe
The hand-foot-genital syndrome: on the variable expression in affected males.
Clinical genetics 1993;43(5):232-4.
1990: J P Fryns; Annick Vogels; Herman Van Den Berghe
Mental retardation, craniofacial dysmorphism, hypogonadism, diabetes mellitus and epilepsy in four siblings. A "new" mental retardation syndrome.
Clinical genetics 1990;37(2):111-6.
1990: J P Fryns; Annick Vogels; Herman Van Den Berghe
Craniosynostosis and low middle frequency perceptive deafness in mother and son. A distinct entity?
Genetic counseling (Geneva, Switzerland) 1990;1(1):63-6.