Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature

Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services

(2013) Jennifer L. Roberts et al.   GENE

Overdosage of Hand2 causes limb and heart defects in the human chromosomal disorder partial trisomy distal 4q

(2013) Masaru Tamura et al.   HUMAN MOLECULAR GENETICS

Angiotensin II induces Fat1 expression/activation and vascular smooth muscle cell migration via Nox1-dependent reactive oxygen species generation

(2013) T. Bruder-Nascimento et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

edn1 and hand2 Interact in Early Regulation of Pharyngeal Arch Outgrowth during Zebrafish Development

(2013) Mark M. Sasaki et al.   PLoS One

Evolution of the Plasma and Tissue Kallikreins, and Their Alternative Splicing Isoforms

(2013) Vassiliki Lila Koumandou et al.   PLoS One

Congenital Factor XI Deficiency: An Update

(2013) Stefano Duga et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Sorbin and SH3 Domain‐Containing Protein 2 Is Released From Infarcted Heart in the Very Early Phase: Proteomic Analysis of Cardiac Tissues From Patients

(2013) Yu Kakimoto et al.   Journal of the American Heart Association

Chromosome 4q deletion syndrome: Narrowing the cardiovascular critical region to 4q32.2-q34.3

(2012) Wenbo Xu et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genotype-phenotype analysis of 4q deletion syndrome: Proposal of a critical region

(2012) Eugen-Matthias Strehle et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The spectrum of 4q- syndrome illustrated by a case series

(2012) Eugen-Matthias Strehle et al.   GENE

Maternal Transmission Effect of a PDGF-C SNP on Nonsyndromic Cleft Lip with or without Palate from a Chinese Population

(2012) Di Wu et al.   PLoS One

Inner ear dysfunction in caspase-3 deficient mice

(2011) Tomoko Makishima et al.   BMC NEUROSCIENCE

12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes

(2011) Erin L. Youngs et al.   CLINICAL DYSMORPHOLOGY

Terminal deletion of the long arm of chromosome 4 in a mother and two sons

(2010) Maria Descartes et al.   CLINICAL GENETICS

Case Report: Two newborns with chromosome 4 imbalances: deletion 4q33 → q35 and ring r (4) (pterq35.2-qter)

(2010) G. Calabrese et al.   CLINICAL GENETICS

Identification and molecular characterization of two novel chromosomal deletions associated with autism

(2010) W-H Chien et al.   CLINICAL GENETICS

Melody, an ENU mutation in Caspase 3, alters the catalytic cysteine residue and causes sensorineural hearing loss in mice

(2010) Andrew Parker et al.   MAMMALIAN GENOME

Fine-scale recombination rate differences between sexes, populations and individuals

(2010) Augustine Kong et al.   NATURE

Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: Study of two cases and review of the literature

(2009) Michael R. Rossi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Investigation of 4q-deletion in two unrelated patients using array CGH

(2008) S.S. Kaalund et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mutations in mammalian tolloid-like 1 gene detected in adult patients with ASD

(2008) Paweł Stańczak et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Distal del(4) (q33) syndrome: Detailed clinical presentation and molecular description with array-CGH

(2007) Sofia Kitsiou-Tzeli et al.   European Journal of Medical Genetics