Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome

CHD7mutations in patients initially diagnosed with Kallmann syndrome - the clinical overlap with CHARGE syndrome

(2009) MCJ Jongmans et al.   CLINICAL GENETICS

Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns

(2009) M. P. Schnetz et al.   GENOME RESEARCH

Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

(2008) Hyung-Goo Kim et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Olfactory Anomalies in CHARGE Syndrome: Imaging Findings of a Potential Major Diagnostic Criterion

(2008) J. Blustajn et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

A familial CHARGE syndrome with a CHD7 nonsense mutation and new clinical features

(2008) Pia E. Vuorela et al.   CLINICAL DYSMORPHOLOGY

Anterior-posterior graded response to Otx2 controls proliferation and differentiation of dopaminergic progenitors in the ventral mesencephalon

(2008) D. Omodei et al.   DEVELOPMENT

Horizontal Basal Cells Are Multipotent Progenitors in Normal and Injured Adult Olfactory Epithelium

(2008) Naomi Iwai et al.   STEM CELLS

Drosophila Kismet Regulates Histone H3 Lysine 27 Methylation and Early Elongation by RNA Polymerase II

(2008) Shrividhya Srinivasan et al.   PLoS Genetics

Endocrine and Radiological Studies in Patients with Molecularly Confirmed CHARGE Syndrome

(2007) Yumi Asakura et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM