A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features

Cdh1 controls the stability of TACC3

(2011) Jen-Chong Jeng et al.   CELL CYCLE

Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay

(2010) Femke Hannes et al.   European Journal of Medical Genetics

De novo rates and selection of large copy number variation

(2010) A. Itsara et al.   GENOME RESEARCH

Inv dup del(4)(:p13 → p16.3::p16.3 → qter) in a girl without typical manifestations of Wolf-Hirschhorn syndrome

(2009) Giorgio A. Paskulin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genomic duplication ofPTPN11is an uncommon cause of Noonan syndrome

(2009) John M. Graham et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Submicroscopic Duplication of the Wolf-Hirschhorn Critical Region with a 4p Terminal Deletion

(2009) M. Roselló et al.   CYTOGENETIC AND GENOME RESEARCH

Fibroblast growth factor (FGF) gene expression in the developing cerebellum suggests multiple roles for FGF signaling during cerebellar morphogenesis and development

(2009) Yuichiro Yaguchi et al.   DEVELOPMENTAL DYNAMICS

Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome

(2008) Oleg A. Shchelochkov et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3

(2008) Sarah T. South et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Characterization of the mitochondrial protein LETM1, which maintains the mitochondrial tubular shapes and interacts with the AAA-ATPase BCS1L

(2008) S. Tamai et al.   JOURNAL OF CELL SCIENCE

The TACC proteins: TACC-ling microtubule dynamics and centrosome function

(2008) Isabel Peset et al.   TRENDS IN CELL BIOLOGY