An atypical 7q11.23 deletion in a normal IQ Williams–Beuren syndrome patient

Is it Williams syndrome?GTF2IRD1implicated in visual-spatial construction andGTF2Iin sociability revealed by high resolution arrays

(2009) L. Dai et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Infantile Spasms Is Associated with Deletion of the MAGI2 Gene on Chromosome 7q11.23-q21.11

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The common inversion of the Williams–Beuren syndrome region at 7q11.23 does not cause clinical symptoms

(2008) Elaine Tam et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Williams–Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase

(2008) Lucia Micale et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Identification of the TFII-I family target genes in the vertebrate genome

(2008) Nyam-Osor Chimge et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development

(2008) B. Enkhmandakh et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development

(2008) Alyson Ashe et al.   GENOME BIOLOGY