Velo-cardio-facial syndrome (VCFS), also known as 22q11.2 deletion syndrome, is a common genetic condition associated with increased risk for developing schizophrenia. Given that cortical malformations play an integral role in the pattern of neuroanatomical alterations associated with VCFS, the aim of the present study was to quantify and localize gyral abnormalities. Magnetic resonance images were obtained on a 1.5 T scanner. The gyrification index (GI), a measure of the degree of cortical complexity, was differentially calculated for each lobe using a semi-automated protocol. The GI was calculated for 37 patients affected by VCFS as well as for 36 comparison individuals group-matched for age, handedness, and gender. The subjects affected ...
Introduction Subjects with 22q11.2 deletion syndrome (22g11 DS) and subjects with ultra-high risk fo...
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder associated with neurocog...
Background: Velo-cardio-facial syndrome (VCFS, MIM#192430, 22q11.2 Deletion Syndrome) is a genetic d...
Introduction: Velo-cardio-facial syndrome (VCFS) has been identified as an important risk factor for...
Objective: Velo-cardio-facial syndrome (VCFS; 22q11.2 deletion syndrome) represents one of the highe...
BACKGROUND: Velo-cardio-facial syndrome (VCFS) is associated with deletions in the qll band of chro...
Abstract Background Velo-cardio-facial syndrome (VCFS, MIM#192430, 22q11.2 Deletion Syndrome) is a g...
OBJECTIVES: 22q11.2 deletion syndrome (22q11.2DS), also known as velocardiofacial syndrome (VCFS) or...
BACKGROUND: Individuals with velocardio-facial syndrome (VCFS), a genetic disorder associated with m...
The 22q11.2 deletion syndrome (velocardiofacial/DiGeorge syn-drome) is a neurogenetic condition asso...
Velo-cardio-facial syndrome (VCFS) is a genetic disorder associated with 22q11 deletion, a character...
Approximately 30% of individuals with 22q11.2 Deletion Syndrome (22q11DS) develop schizophrenia duri...
BACKGROUND: As children with velocardiofacial syndrome (VCFS) develop, they are at increased risk fo...
The 22q11.2 deletion syndrome (velocardiofacial/DiGeorge syn-drome, 22q11.2DS) involves cardiac and ...
Background: Up to 30% of young adults with velocardiofacial syndrome (VCFS; 22q11.2 deletion syndrom...
Introduction Subjects with 22q11.2 deletion syndrome (22g11 DS) and subjects with ultra-high risk fo...
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder associated with neurocog...
Background: Velo-cardio-facial syndrome (VCFS, MIM#192430, 22q11.2 Deletion Syndrome) is a genetic d...
Introduction: Velo-cardio-facial syndrome (VCFS) has been identified as an important risk factor for...
Objective: Velo-cardio-facial syndrome (VCFS; 22q11.2 deletion syndrome) represents one of the highe...
BACKGROUND: Velo-cardio-facial syndrome (VCFS) is associated with deletions in the qll band of chro...
Abstract Background Velo-cardio-facial syndrome (VCFS, MIM#192430, 22q11.2 Deletion Syndrome) is a g...
OBJECTIVES: 22q11.2 deletion syndrome (22q11.2DS), also known as velocardiofacial syndrome (VCFS) or...
BACKGROUND: Individuals with velocardio-facial syndrome (VCFS), a genetic disorder associated with m...
The 22q11.2 deletion syndrome (velocardiofacial/DiGeorge syn-drome) is a neurogenetic condition asso...
Velo-cardio-facial syndrome (VCFS) is a genetic disorder associated with 22q11 deletion, a character...
Approximately 30% of individuals with 22q11.2 Deletion Syndrome (22q11DS) develop schizophrenia duri...
BACKGROUND: As children with velocardiofacial syndrome (VCFS) develop, they are at increased risk fo...
The 22q11.2 deletion syndrome (velocardiofacial/DiGeorge syn-drome, 22q11.2DS) involves cardiac and ...
Background: Up to 30% of young adults with velocardiofacial syndrome (VCFS; 22q11.2 deletion syndrom...
Introduction Subjects with 22q11.2 deletion syndrome (22g11 DS) and subjects with ultra-high risk fo...
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder associated with neurocog...
Background: Velo-cardio-facial syndrome (VCFS, MIM#192430, 22q11.2 Deletion Syndrome) is a genetic d...