Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability.
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[1] G Mortier,et al. Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports , 2006, Journal of Medical Genetics.
[2] Bassem A Bejjani,et al. Clinical utility of contemporary molecular cytogenetics. , 2008, Annual review of genomics and human genetics.
[3] Richard R Sharp,et al. Evaluating the utility of personal genomic information , 2009, Genetics in Medicine.
[4] Juliane Hoyer,et al. Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation , 2006, American journal of medical genetics. Part A.
[5] Carol A. Marra,et al. Valuing the benefit of diagnostic testing for genetic causes of idiopathic developmental disability: willingness to pay from families of affected children , 2009, Clinical genetics.
[6] M. Khoury,et al. Personal utility and genomic information: Look before you leap , 2009, Genetics in Medicine.
[7] M. Drummond,et al. Health Care Technology: Effectiveness, Efficiency and Public Policy@@@Methods for the Economic Evaluation of Health Care Programmes , 1988 .
[8] Y J Crow,et al. Recurrence risks in mental retardation. , 1998, Journal of medical genetics.
[9] N. Carter,et al. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents , 2005, Journal of Medical Genetics.
[10] Nel Roeleveld,et al. The prevalence of mental retardation: a critical review of recent literature , 1997, Developmental medicine and child neurology.
[11] R. Hennekam,et al. Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience , 2002, Journal of medical genetics.
[12] Sarah Barber,et al. Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation. , 2006, American journal of human genetics.
[13] C. Ruivenkamp,et al. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH) , 2005, Journal of Medical Genetics.
[14] Naomichi Matsumoto,et al. BAC array CGH reveals genomic aberrations in idiopathic mental retardation , 2006, American journal of medical genetics. Part A.
[15] Ton Feuth,et al. Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities. , 2003, American journal of human genetics.
[16] Ton Feuth,et al. Diagnostic genome profiling in mental retardation. , 2005, American journal of human genetics.
[17] M Somerville,et al. Submicroscopic deletions and duplications in individuals with intellectual disability detected by array‐CGH , 2005, American journal of medical genetics. Part A.
[18] Toshiyuki Yamamoto,et al. Application of array-based comparative genome hybridization in children with developmental delay or mental retardation. , 2008, Pediatrics and neonatology.
[19] Dean A. Regier,et al. Evaluating health-related quality-of-life studies in paediatric populations , 2012, PharmacoEconomics.
[20] A. Briggs,et al. Probabilistic Sensitivity Analysis for Decision Trees with Multiple Branches: Use of the Dirichlet Distribution in a Bayesian Framework , 2003, Medical decision making : an international journal of the Society for Medical Decision Making.
[21] M. Sculpher,et al. Decision Modelling for Health Economic Evaluation , 2006 .
[22] Martin Offringa,et al. Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness , 2005, European Journal of Human Genetics.
[23] Simon Sanderson,et al. Array-based comparative genomic hybridization for investigating chromosomal abnormalities in patients with learning disability: Systematic review meta-analysis of diagnostic and false-positive yields , 2007, Genetics in Medicine.
[24] W. Sloos,et al. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations , 2006, Cytogenetic and Genome Research.
[25] F. Zahir,et al. The impact of array genomic hybridization on mental retardation research: a review of current technologies and their clinical utility , 2007, Clinical genetics.
[26] K. Hirschhorn,et al. Clinical Utility of Array CGH for the Detection of Chromosomal Imbalances Associated with Mental Retardation and Multiple Congenital Anomalies , 2009, Annals of the New York Academy of Sciences.
[27] M. Gingold,et al. CME Practice parameter : Evaluation of the child with global developmental delay , 2003 .
[28] M Bobrow,et al. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features , 2004, Journal of Medical Genetics.
[29] D. Ledbetter,et al. Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities , 2005, Journal of Medical Genetics.
[30] A S Detsky,et al. How attractive does a new technology have to be to warrant adoption and utilization? Tentative guidelines for using clinical and economic evaluations. , 1992, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.