Aetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old children

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

(2010) David T. Miller et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Rett syndrome: Revised diagnostic criteria and nomenclature

(2010) Jeffrey L. Neul et al.   ANNALS OF NEUROLOGY

High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical setting

(2010) J Wincent et al.   CLINICAL GENETICS

Aetiological factors and prevalence of severe mental retardation in children in a Swedish municipality: the possible role of consanguinity

(2010) Elisabeth Fernell   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

THE AETIOLOGY OF INTELLECTUAL DISABILITY IN WESTERN AUSTRALIA: A COMMUNITY-BASED STUDY

(2010) Diana Wellesley et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

(2010) Melanie Manning et al.   GENETICS IN MEDICINE

Clinical Genetic Testing for Patients With Autism Spectrum Disorders

(2010) Y. Shen et al.   PEDIATRICS

Identification of critical regions for clinical features of distal 10q deletion syndrome

(2009) SA Yatsenko et al.   CLINICAL GENETICS

A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients

(2009) Hartmut Engels et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis

(2009) L. E. L. M. Vissers et al.   JOURNAL OF MEDICAL GENETICS

Sex differences in the evaluation and diagnosis of autism spectrum disorders among children

(2009) Ellen Giarelli et al.   Disability and Health Journal

Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion

(2008) C. Cardoso et al.   NEUROLOGY