Identification of a Novel ENU-Induced Mutation in Mouse Tbx1 Linked to Human DiGeorge Syndrome

Cortical Development Requires Mesodermal Expression ofTbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome

(2016) Gemma Flore et al.   CEREBRAL CORTEX

Rebalancing gene haploinsufficiency in vivo by targeting chromatin

(2016) Filomena Gabriella Fulcoli et al.   Nature Communications

A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome

(2014) Jennifer C. Fuchs et al.   HUMAN MOLECULAR GENETICS

TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia

(2014) Tsutomu Ogata et al.   PLoS One

A gradient of Bmp7 specifies the tonotopic axis in the developing inner ear

(2014) Zoë F. Mann et al.   Nature Communications

TMHS Is an Integral Component of the Mechanotransduction Machinery of Cochlear Hair Cells

(2012) Wei Xiong et al.   CELL

Genetics

(2012) A. Eliot Shearer et al.   CURRENT OPINION IN PEDIATRICS

How the Genetics of Deafness Illuminates Auditory Physiology

(2011) Guy P. Richardson et al.   Annual Review of Physiology

HIF–VEGF Pathways Are Critical for Chronic Otitis Media in Junbo and Jeff Mouse Mutants

(2011) Michael T. Cheeseman et al.   PLoS Genetics

Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice

(2011) Jennifer M Hilton et al.   GENOME BIOLOGY

Mutation discovery in mice by whole exome sequencing

(2011) Heather Fairfield et al.   GENOME BIOLOGY

A catechol-O-methyltransferase that is essential for auditory function in mice and humans

(2008) X. Du et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA