22q11.2 Deletions in Patients with Conotruncal Defects: Data from 1,610 Consecutive Cases

Variation in prevalence of chromosome 22q11 deletion in subtypes of conotruncal defect in 254 children

(2011) A Anilkumar et al.   ACTA PAEDIATRICA

The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study

(2011) Peter Agergaard et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Association of Schizophrenia in 22q11.2 Deletion Syndrome and Gray Matter Volumetric Deficits in the Superior Temporal Gyrus

(2011) Eva W.C. Chow et al.   AMERICAN JOURNAL OF PSYCHIATRY

Cognitive, Behavioural and Psychiatric Phenotype in 22q11.2 Deletion Syndrome

(2011) Nicole Philip et al.   BEHAVIOR GENETICS

Evolving applications of microarray analysis in prenatal diagnosis

(2011) Melissa S Savage et al.   CURRENT OPINION IN OBSTETRICS & GYNECOLOGY

From Karyotyping to Array-CGH in Prenatal Diagnosis

(2011) K.D. Lichtenbelt et al.   CYTOGENETIC AND GENOME RESEARCH

Cardiovascular Anomalies Associated With Chromosome 22q11.2 Deletion Syndrome

(2010) Kazuo Momma   AMERICAN JOURNAL OF CARDIOLOGY

Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review

(2010) Peter Agergaard et al.   European Journal of Medical Genetics

Applications of Array Comparative Genomic Hybridization in Obstetrics

(2010) Gary Fruhman et al.   OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA

Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting

(2010) Idit Maya et al.   PRENATAL DIAGNOSIS

Familial transposition of the great arteries caused by multiple mutations in laterality genes

(2009) A. De Luca et al.   HEART

ACOG Committee Opinion No. 446: Array Comparative Genomic Hybridization in Prenatal Diagnosis

(2009)   OBSTETRICS AND GYNECOLOGY

Do Neonates with Genetic Abnormalities Have an Increased Morbidity and Mortality following Cardiac Surgery?

(2009) Janet M. Simsic et al.   Congenital Heart Disease

Genetic counseling for the 22q11.2 deletion

(2008) Donna M. McDonald-McGinn et al.   Developmental Disabilities Research Reviews

Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery

(2008) Lidia Ziolkowska et al.   EUROPEAN JOURNAL OF PEDIATRICS

High-resolution array genomic hybridization in prenatal diagnosis

(2008) J. M. Friedman   PRENATAL DIAGNOSIS