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Journal of Mental Deficiency Research
|
June 1, 1990
The 49,XXXXY syndrome: clinical and psychological findings in five patients
L M Curfs, G Schreppers-Tijdink, A Wiegers, et al.
Journal of Medical Genetics
|
July 1, 1989
Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys
L M Curfs, G Schreppers-Tijdink, A Wiegers, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features
A M Wiegers, L M Curfs, H Meijer, et al.
Clinical Genetics
|
December 1, 1991
Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome
L M Curfs, A M Wiegers, J R Sommers, et al.
Journal De Genetique Humaine
|
December 1, 1988
A systematic cytogenetic study of a population of 1170 mentally retarded and/or behaviourly disturbed patients including fragile X-screening. The Hondsberg experience
G A Schreppers-Tijdink, L M Curfs, A Wiegers, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
August 5, 1998
Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome
C F van Lieshout, R E De Meyer, L M Curfs, et al.
Clinical Genetics
|
December 1, 1989
Strengths and weaknesses in the cognitive profile of fra(X) patients
L M Curfs, M Borghgraef, A Wiegers, et al.
Journal of Intellectual Disability Research : JIDR
|
February 25, 1999
Prader-Willi syndrome and psychotic symptoms: 1. Case descriptions and genetic studies
D Clarke, H Boer, T Webb, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
The Prader-Willi syndrome: a self supporting program for children, youngsters and adults
M J Descheemaeker, A Swillen, L Plissart, et al.
Journal of Pediatric Psychology
|
May 20, 1998
Problem behaviors and personality of children and adolescents with Prader-Willi syndrome
C F van Lieshout, R E de Meyer, L M Curfs, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
Journal of Mental Deficiency Research
|
June 1, 1990
The 49,XXXXY syndrome: clinical and psychological findings in five patients
L M Curfs, G Schreppers-Tijdink, A Wiegers, et al.
Journal of Medical Genetics
|
July 1, 1989
Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys
L M Curfs, G Schreppers-Tijdink, A Wiegers, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features
A M Wiegers, L M Curfs, H Meijer, et al.
Clinical Genetics
|
December 1, 1991
Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome
L M Curfs, A M Wiegers, J R Sommers, et al.
Journal De Genetique Humaine
|
December 1, 1988
A systematic cytogenetic study of a population of 1170 mentally retarded and/or behaviourly disturbed patients including fragile X-screening. The Hondsberg experience
G A Schreppers-Tijdink, L M Curfs, A Wiegers, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
August 5, 1998
Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome
C F van Lieshout, R E De Meyer, L M Curfs, et al.
Clinical Genetics
|
December 1, 1989
Strengths and weaknesses in the cognitive profile of fra(X) patients
L M Curfs, M Borghgraef, A Wiegers, et al.
Journal of Intellectual Disability Research : JIDR
|
February 25, 1999
Prader-Willi syndrome and psychotic symptoms: 1. Case descriptions and genetic studies
D Clarke, H Boer, T Webb, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
The Prader-Willi syndrome: a self supporting program for children, youngsters and adults
M J Descheemaeker, A Swillen, L Plissart, et al.
Journal of Pediatric Psychology
|
May 20, 1998
Problem behaviors and personality of children and adolescents with Prader-Willi syndrome
C F van Lieshout, R E de Meyer, L M Curfs, et al.
Page
of 3