✦ LIBER ✦

Disturbed cortical gyrification in 22q11 deletion syndrome: Potential cues to the etiology of brain malformations in the syndrome

✍ Scribed by M. Schaer; M. Bach Cuadra; B. Glaser; M. Debbané; J.-P. Thiran; S. Eliez

Book ID: 119363390
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 65 KB
Volume: 98
Category: Article
ISSN: 0920-9964
DOI: 10.1016/j.schres.2007.12.031

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Polymicrogyria and deletion 22q11.2 synd

Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation

✍ Nathaniel H. Robin; Clare J. Taylor; Donna M. McDonald-McGinn; Elaine H. Zackai; 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 331 KB 👁 2 views

Evaluation of potential modifiers of the

Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome

✍ Elizabeth Goldmuntz; Deborah A. Driscoll; Beverly S. Emanuel; Donna McDonald-McG 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 76 KB

## Abstract ## BACKGROUND: The phenotype associated with deletion of the 22q11.2 chromosomal region is highly variable, yet little is known about the source of this variability. Cardiovascular anomalies, including tetralogy of Fallot, truncus arteriosus, interrupted aortic arch type B, perimembran

Visual scanning of faces in 22q11.2 dele

Visual scanning of faces in 22q11.2 deletion syndrome: Attention to the mouth or the eyes?

✍ Linda Campbell; Kathryn McCabe; Kate Leadbeater; Ulrich Schall; Carmel Loughland 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 163 KB

Volumetric, connective, and morphologic

Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study

✍ Simon, Tony J.; Ding, Lijun; Bish, Joel P.; McDonald-McGinn, Donna M.; Zackai, E 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 631 KB

A candidate gene approach to identify mo

A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients

✍ Josine C.C. Widdershoven; Mark Bowser; Molly B. Sheridan; Donna M. McDonald-McGi 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 180 KB

Poster #S15 A MOUSE MODEL OF 22Q11 DELET

Poster #S15 A MOUSE MODEL OF 22Q11 DELETION SYNDROME EXHIBITS DEFICITS IN BEHAVIORS RELEVANT TO THE CORE DOMAINS OF SCHIZOPHRENIA

✍ Hughes, Zoe A.; Graf, Radka; Hanks, Ashley; Lotarski, Susan; More, Alexander I.; 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 88 KB