Deletion 2p15-16.1 syndrome: Case report and review

TBX2 gene duplication associated with complex heart defect and skeletal malformations

(2010) Francesca Clementina Radio et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Zellweger syndrome caused by PEX13 deficiency: Report of two novel mutations

(2009) O.Y. Al-Dirbashi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

2q31.2q32.3 deletion syndrome: Report of an adult patient

(2009) Paolo Prontera et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion

(2009) J-S Liang et al.   JOURNAL OF MEDICAL GENETICS

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases

(2008) Lina Shao et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clinical Utility of Array CGH for the Detection of Chromosomal Imbalances Associated with Mental Retardation and Multiple Congenital Anomalies

(2008) Lisa Edelmann et al.   Annals of the New York Academy of Sciences