A rare 3q13.31 microdeletion including GAP43 and LSAMP genes

Growth Associated Protein 43 Is Expressed in Skeletal Muscle Fibers and Is Localized in Proximity of Mitochondria and Calcium Release Units

(2013) Simone Guarnieri et al.   PLoS One

A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

(2011) A-M Molin et al.   JOURNAL OF MEDICAL GENETICS

Recurrent Focal Copy-Number Changes and Loss of Heterozygosity Implicate Two Noncoding RNAs and One Tumor Suppressor Gene at Chromosome 3q13.31 in Osteosarcoma

(2010) I. Pasic et al.   CANCER RESEARCH

Resistance to change and vulnerability to stress: autistic-like features of GAP43-deficient mice

(2010) K. J. Zaccaria et al.   GENES BRAIN AND BEHAVIOR

A de novo 1.9-Mb interstitial deletion of 3q13.2q13.31 in a girl with dysmorphic features, muscle hypotonia, and developmental delay

(2009) Keiko Shimojima et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Polymorphisms of the Tumor Suppressor Gene LSAMP are Associated with Left Main Coronary Artery Disease

(2008) L. Wang et al.   ANNALS OF HUMAN GENETICS

A high-density SNP genome-wide linkage scan in a large autism extended pedigree

(2008) K Allen-Brady et al.   MOLECULAR PSYCHIATRY