A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes

Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes

(2013) Maria Delio et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Fetal heart defects: Potential and pitfalls of first-trimester detection

(2013) Asma Khalil et al.   Seminars in Fetal & Neonatal Medicine

Phenotypic variability of atypical 22q11.2 deletions not includingTBX1

(2012) Judith M.A. Verhagen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genotype-phenotype correlation in 22q11.2 deletion syndrome

(2012) Elena Michaelovsky et al.   BMC Medical Genetics

Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions

(2011) G. Costain et al.   JOURNAL OF MEDICAL GENETICS

A copy number variation morbidity map of developmental delay

(2011) Gregory M Cooper et al.   NATURE GENETICS

Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome

(2010) Florence Bretelle et al.   European Journal of Medical Genetics

Sex differences in the behavior of children with the 22q11 deletion syndrome

(2009) Christina Sobin et al.   PSYCHIATRY RESEARCH

Clinical variability of the 22q11.2 duplication syndrome

(2008) Christian Wentzel et al.   European Journal of Medical Genetics

Schizophrenia and 22q11.2 deletion syndrome

(2008) Anne S. Bassett et al.   Current Psychiatry Reports