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Tijdschrift Voor Psychiatrie
|
October 9, 2010
[Sleep disturbances in Smith-Magenis syndrome: treatment with melatonin and beta-adrenergic antagonists]
A Van Thillo, K Devriendt, D Willekens
Genetic Counseling (Geneva, Switzerland)
|
July 14, 2000
Three young children with Smith-Magenis syndrome: their distinct, recognisable behavioural phenotype as the most important clinical symptoms
D Willekens, P De Cock, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
June 21, 2008
The long term evolution of 6 adult patients with Cohen syndrome and their behavioral characteristics
K Peeters, D Willekens, J Steyaert, et al.
Clinical Genetics
|
September 4, 1998
Marden-Walker syndrome versus isolated distal arthrogryposis: evidence that both conditions may be variable manifestations of the same mutated gene
J P Fryns, D Willekens, D Van Schoubroeck, et al.
Clinical Genetics
|
April 19, 2011
Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated
E Chabchoub, D Willekens, J R Vermeesch, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 6, 2001
Terminal 6q25.3 deletion and abnormal behaviour
T Lukusa, D Willekens, N Lukusa, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 5, 2001
Emotional and behavioral profile and child psychiatric diagnosis in the childhood type of myotonic dystrophy
E Goossens, J Steyaert, C De Die-Smulders, et al.
Journal of Intellectual Disability Research : JIDR
|
February 20, 2002
Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrum
M J Descheemaeker, A Vogels, V Govers, et al.
Clinical Genetics
|
October 23, 1997
A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy
J Steyaert, S Umans, D Willekens, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Tijdschrift Voor Psychiatrie
|
October 9, 2010
[Sleep disturbances in Smith-Magenis syndrome: treatment with melatonin and beta-adrenergic antagonists]
A Van Thillo, K Devriendt, D Willekens
Genetic Counseling (Geneva, Switzerland)
|
July 14, 2000
Three young children with Smith-Magenis syndrome: their distinct, recognisable behavioural phenotype as the most important clinical symptoms
D Willekens, P De Cock, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
June 21, 2008
The long term evolution of 6 adult patients with Cohen syndrome and their behavioral characteristics
K Peeters, D Willekens, J Steyaert, et al.
Clinical Genetics
|
September 4, 1998
Marden-Walker syndrome versus isolated distal arthrogryposis: evidence that both conditions may be variable manifestations of the same mutated gene
J P Fryns, D Willekens, D Van Schoubroeck, et al.
Clinical Genetics
|
April 19, 2011
Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated
E Chabchoub, D Willekens, J R Vermeesch, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 6, 2001
Terminal 6q25.3 deletion and abnormal behaviour
T Lukusa, D Willekens, N Lukusa, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 5, 2001
Emotional and behavioral profile and child psychiatric diagnosis in the childhood type of myotonic dystrophy
E Goossens, J Steyaert, C De Die-Smulders, et al.
Journal of Intellectual Disability Research : JIDR
|
February 20, 2002
Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrum
M J Descheemaeker, A Vogels, V Govers, et al.
Clinical Genetics
|
October 23, 1997
A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy
J Steyaert, S Umans, D Willekens, et al.
Page
of 1