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Journal of Developmental and Behavioral Pediatrics : JDBP
|
February 1, 1992
Neurodevelopmental study of writing disorders in middle childhood
A D Sandler, T E Watson, M Footo, et al.
Journal of Intellectual Disability Research : JIDR
|
July 26, 2014
A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders
J Goodwin, K Schoch, V Shashi, et al.
Pediatrics
|
October 4, 2000
Otitis media in childhood in relation to preschool language and school readiness skills among black children
J E Roberts, M R Burchinal, S C Jackson, et al.
Journal of Intellectual Disability Research : JIDR
|
April 15, 2015
Social cognitive training in adolescents with chromosome 22q11.2 deletion syndrome: feasibility and preliminary effects of the intervention
V Shashi, W Harrell, S Eack, et al.
Pediatrics
|
August 1, 1998
Otitis media, the caregiving environment, and language and cognitive outcomes at 2 years
J E Roberts, M R Burchinal, S A Zeisel, et al.
The Journal of Pediatrics
|
January 1, 1993
Neuropsychologic functioning of human immunodeficiency virus-infected children with hemophilia
J K Whitt, S R Hooper, M B Tennison, et al.
Translational Psychiatry
|
July 27, 2012
Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome
R Das Chakraborty, D Chakraborty, A J Bernal, et al.
Journal of Pediatric Nursing
|
July 27, 2015
Self-Management and Transition Readiness Assessment: Development, Reliability, and Factor Structure of the STARx Questionnaire
M Ferris, S Cohen, C Haberman, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
June 20, 2019
Altered Brain Structure in Infants with Turner Syndrome
M L Davenport, E Cornea, K Xia, et al.
Translational Psychiatry
|
February 22, 2017
No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients
M Guipponi, F Santoni, M Schneider, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Journal of Developmental and Behavioral Pediatrics : JDBP
|
February 1, 1992
Neurodevelopmental study of writing disorders in middle childhood
A D Sandler, T E Watson, M Footo, et al.
Journal of Intellectual Disability Research : JIDR
|
July 26, 2014
A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders
J Goodwin, K Schoch, V Shashi, et al.
Pediatrics
|
October 4, 2000
Otitis media in childhood in relation to preschool language and school readiness skills among black children
J E Roberts, M R Burchinal, S C Jackson, et al.
Journal of Intellectual Disability Research : JIDR
|
April 15, 2015
Social cognitive training in adolescents with chromosome 22q11.2 deletion syndrome: feasibility and preliminary effects of the intervention
V Shashi, W Harrell, S Eack, et al.
Pediatrics
|
August 1, 1998
Otitis media, the caregiving environment, and language and cognitive outcomes at 2 years
J E Roberts, M R Burchinal, S A Zeisel, et al.
The Journal of Pediatrics
|
January 1, 1993
Neuropsychologic functioning of human immunodeficiency virus-infected children with hemophilia
J K Whitt, S R Hooper, M B Tennison, et al.
Translational Psychiatry
|
July 27, 2012
Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome
R Das Chakraborty, D Chakraborty, A J Bernal, et al.
Journal of Pediatric Nursing
|
July 27, 2015
Self-Management and Transition Readiness Assessment: Development, Reliability, and Factor Structure of the STARx Questionnaire
M Ferris, S Cohen, C Haberman, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
June 20, 2019
Altered Brain Structure in Infants with Turner Syndrome
M L Davenport, E Cornea, K Xia, et al.
Translational Psychiatry
|
February 22, 2017
No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients
M Guipponi, F Santoni, M Schneider, et al.
Page
of 5