Search research articles
Contact Us
Filters
Showing results (31-40 of 98) with videos related to
Page
of 10
Sort By:
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence
|
April 13, 2005
Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome
Peter Stiers, Ann Swillen, Bert De Smedt, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndrome
Elke Loos, Nicolas Verhaert, Annelore Willaert, et al.
BMC Pediatrics
|
May 7, 2026
Time poverty of families of children with 22q11DS: a healthcare professional perspective
Sophie Ayoub, Eva De Clercq, Sandra Meier, et al.
Health Care Transitions
|
October 2, 2025
Transition services in 22q11 deletion syndrome: Hit or miss
Sophie Ayoub, Sandra Meier, Cheryl Cytrynbaum, et al.
American Journal of Medical Genetics. Part A
|
May 2, 2023
Triplications of chromosome 1p36.3, including the genes GABRD and SKI, are associated with a developmental disorder and a facial gestalt
Elise Pelgrims, Sally Ann Lynch, Laurens Hannes, et al.
Journal of Speech, Language, and Hearing Research : JSLHR
|
June 2, 2016
Prevalence and Nature of Hearing Loss in 22q11.2 Deletion Syndrome
Charlotte Van Eynde, Ann Swillen, Elien Lambeens, et al.
Developmental Medicine and Child Neurology
|
March 16, 2007
Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)
Katrijn Van Aken, Bert De Smedt, Annelies Van Roie, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry
|
December 2, 2021
Blood brain barrier permeability increases with age in individuals with 22q11.2 deletion syndrome
Michal Taler, Ehud Mekori-Domachevsky, Elfi Vergaelen, et al.
Brain, Behavior, and Immunity
|
August 4, 2023
The relationship between oxidative stress and psychotic disorders in 22q11.2 deletion syndrome
Noam Matalon, Elfi Vergaelen, Shachar Shani, et al.
Journal of Neurodevelopmental Disorders
|
November 28, 2025
The importance of intrafamilial cognitive phenotyping by the case of 22q11.2 deletion, 15q11.2 deletion, and families with inherited copy number variants of unknown significance
Elise Pelgrims, Laurens Hannes, Ilse Noens, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 98) with videos related to
Sort By:
Page
of 10
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence
|
April 13, 2005
Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome
Peter Stiers, Ann Swillen, Bert De Smedt, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndrome
Elke Loos, Nicolas Verhaert, Annelore Willaert, et al.
BMC Pediatrics
|
May 7, 2026
Time poverty of families of children with 22q11DS: a healthcare professional perspective
Sophie Ayoub, Eva De Clercq, Sandra Meier, et al.
Health Care Transitions
|
October 2, 2025
Transition services in 22q11 deletion syndrome: Hit or miss
Sophie Ayoub, Sandra Meier, Cheryl Cytrynbaum, et al.
American Journal of Medical Genetics. Part A
|
May 2, 2023
Triplications of chromosome 1p36.3, including the genes GABRD and SKI, are associated with a developmental disorder and a facial gestalt
Elise Pelgrims, Sally Ann Lynch, Laurens Hannes, et al.
Journal of Speech, Language, and Hearing Research : JSLHR
|
June 2, 2016
Prevalence and Nature of Hearing Loss in 22q11.2 Deletion Syndrome
Charlotte Van Eynde, Ann Swillen, Elien Lambeens, et al.
Developmental Medicine and Child Neurology
|
March 16, 2007
Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)
Katrijn Van Aken, Bert De Smedt, Annelies Van Roie, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry
|
December 2, 2021
Blood brain barrier permeability increases with age in individuals with 22q11.2 deletion syndrome
Michal Taler, Ehud Mekori-Domachevsky, Elfi Vergaelen, et al.
Brain, Behavior, and Immunity
|
August 4, 2023
The relationship between oxidative stress and psychotic disorders in 22q11.2 deletion syndrome
Noam Matalon, Elfi Vergaelen, Shachar Shani, et al.
Journal of Neurodevelopmental Disorders
|
November 28, 2025
The importance of intrafamilial cognitive phenotyping by the case of 22q11.2 deletion, 15q11.2 deletion, and families with inherited copy number variants of unknown significance
Elise Pelgrims, Laurens Hannes, Ilse Noens, et al.
Page
of 10