The 3q29 microdeletion syndrome: Report of three new unrelated patients and in silico “RNA binding” analysis of the 3q29 region

Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review

(2010) Fabiola Quintero-Rivera et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Regulation of mRNA Translation and Stability by microRNAs

(2010) Marc Robert Fabian et al.   Annual Review of Biochemistry

Solving the RIDDLE of 53BP1 recruitment to sites of damage

(2010) Grant S. Stewart   CELL CYCLE

Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder

(2010) Jill Clayton-Smith et al.   CLINICAL DYSMORPHOLOGY

An uncommon 3.4-Mb interstitial deletion at 3q29

(2010) Jia-Chi Wang et al.   CLINICAL DYSMORPHOLOGY

Small RNA-Mediated Gene Regulation in Neurodevelopmental Disorders

(2010) Abrar Qurashi et al.   Current Psychiatry Reports

3q29 microdeletion: A mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairs

(2009) Maria Cristina Digilio et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

RNF168, a new RING finger, MIU-containing protein that modifies chromatin by ubiquitination of histones H2A and H2AX

(2009) Sabrina Pinato et al.   BMC MOLECULAR BIOLOGY

The RIDDLE Syndrome Protein Mediates a Ubiquitin-Dependent Signaling Cascade at Sites of DNA Damage

(2009) Grant S. Stewart et al.   CELL

DNA double strand break repair defects, primary immunodeficiency disorders, and ‘radiosensitivity’

(2009) Shareef A Nahas et al.   Current Opinion in Allergy and Clinical Immunology

1.6Mb deletion in chromosome band 3q29 associated with eye abnormalities

(2009) Nataliya Tyshchenko et al.   European Journal of Medical Genetics

3q29 interstitial microdeletion syndrome: An inherited case associated with cardiac defect and normal cognition

(2009) Feng Li et al.   European Journal of Medical Genetics

A 9.3Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb

(2009) M. Pollazzon et al.   European Journal of Medical Genetics

Small regulatory RNAs in neurodevelopmental disorders

(2009) S. Chang et al.   HUMAN MOLECULAR GENETICS

Biogenesis of small RNAs in animals

(2009) V. Narry Kim et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases

(2008) Lina Shao et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The four mammalian splice variants encoded by the p21-activated kinase 3 gene have different biological properties

(2008) Patricia Kreis et al.   JOURNAL OF NEUROCHEMISTRY

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model

(2008) Kimberly L Stark et al.   NATURE GENETICS

Small non-coding RNAs in animal development

(2008) Giovanni Stefani et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

(2008) Blake C Ballif et al.   Molecular Cytogenetics

Prediction of RNA binding sites in a protein using SVM and PSSM profile

(2007) Manish Kumar et al.   PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS