Deletion of 14.7 Mb 2q32.3q33.3 with a marfanoid phenotype and hypothyroidism

Fetal growth restriction: current knowledge to the general Obs/Gyn

(2012) Luciano Marcondes Machado Nardozza et al.   ARCHIVES OF GYNECOLOGY AND OBSTETRICS

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow

(2011) Malgorzata Srebniak et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype

(2011) M. Balasubramanian et al.   JOURNAL OF MEDICAL GENETICS

Satb1 Ablation Alters Temporal Expression of Immediate Early Genes and Reduces Dendritic Spine Density during Postnatal Brain Development

(2011) M. A. Balamotis et al.   MOLECULAR AND CELLULAR BIOLOGY

The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment

(2010) Alessandro Cocchella et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndrome

(2009) Laila Rifai et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Intrauterine growth restriction: comparison of American College of Obstetricians and Gynecologists practice bulletin with other national guidelines

(2009) Suneet P. Chauhan et al.   AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

Another patient with a de novo deletion further delineates the 2q33.1 microdeletion syndrome

(2009) Thomy J. de Ravel et al.   European Journal of Medical Genetics

Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome

(2009) Jill A. Rosenfeld et al.   PLoS One

Clinical Outcomes of Pulmonary Arterial Hypertension in Carriers ofBMPR2Mutation

(2008) Benjamin Sztrymf et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Identification of human haploinsufficient genes and their genomic proximity to segmental duplications

(2008) Vinh T Dang et al.   EUROPEAN JOURNAL OF HUMAN GENETICS